Sample Handling in California

TICKERWORKS, INC. manufactures precision pharmaceutical compounding and unit-dose drug packaging solutions for human and veterinary pharmacy applications. The company specializes in innovative applicators, dispensers, and molds designed to improve accuracy, reduce waste, and enhance medication delivery. Core product lines include TICKER® click dispensers for transdermal and topical applications, TROCHE POPS® unit-dose pods for sublingual troches, Pebble Beach and RDT molds for rapid-dissolving tablets and troches, suppository molds in various formulations, and compounding kits. The company also offers lab equipment including centrifuges. TICKERWORKS serves compounding pharmacies, veterinary clinics, and compounding professionals, with particular focus on hormone specialists and animal health practitioners. The organization is ISO 9001 certified and FDA registered, indicating compliance with quality management and regulatory standards for pharmaceutical manufacturing. Products emphasize accuracy, eco-friendly design (30% less plastic than comparable dispensers), and ease of use for pharmacy professionals. The company participates actively in professional conferences including ACVP, WVC, and industry owner summits, indicating strong market positioning within pharmacy and veterinary communities.

ApplyLabWork Inc. is a supplier of engineered 3D printing resins for vat polymerization printers, serving dental, jewelry, medical device prototyping, and industrial design markets. The company manufactures photopolymer resins optimized for multiple printing technologies including Laser/SLA (405nm UV), DLP (Digital Light Processing projector-based), and MSLA (Masked LCD-over-LED array) platforms. Product lines include biocompatible resins certified to ISO 10993-5 standards (Tray Orange, BioModeling Gray/Sand, DLP SG Clear for dental surgical accessories), flexible resins for indirect bonding trays (FLEX BT Translucent), castable resins for jewelry lost-wax casting applications (Castable Plus Black), and design/prototype resins emphasizing high resolution, dimensional accuracy, surface finish, and durability. Featured resins are formulated for specific performance characteristics: Modeling Series for precision and intricate details, Modeling Plus for moderate flexibility with impact resistance, and Prototype Flex for compression/bending simulation mimicking elastomeric materials. The company maintains technical specifications addressing post-curing requirements, material elongation properties (Modeling Plus: 25–35% elongation), and application-specific certifications. ApplyLabWork serves the dental laboratory, medical device development, jewelry manufacturing, and precision engineering sectors. Domestically, the company offers free shipping on US continental orders above $169, military discount pricing, and international shipping options. No regulatory certifications beyond ISO 10993-5 biocompatibility are explicitly mentioned on the site.

Biowy Corporation is a medical device manufacturer headquartered in Lake Forest, California, producing a diversified portfolio of disposable medical devices and biologics. The company manufactures cord blood processing and preservation kits for stem cell banking and regenerative medicine applications, tympanostomy tubes for otologic procedures, percutaneous central catheter (PICC) systems in multiple lumen configurations, midline catheters for vascular access, vascular access ports for long-term infusion therapy, demineralized bone matrix (DBM) products including C-Mix formulations for orthopedic and spinal applications, and hyaluronic acid products. Biowy operates both corporate headquarters and a dedicated manufacturing facility in Lake Forest. The company serves hospitals, surgical centers, otolaryngology and pediatric practices, and healthcare systems requiring single-use sterile medical devices. Products emphasize biocompatible materials, sterile construction, and clinical safety. The company maintains customer service operations with standard business hours Monday–Friday, 8am–5pm PST, and accepts inquiries through multiple channels including email, phone, and web-based contact forms.

SciGene manufactures specialized laboratory equipment for cytogenetics and molecular pathology applications. The company produces thermal incubators, tissue/specimen processors, and FISH (Fluorescence In Situ Hybridization) reagents and consumables. Primary products include the Hybex Incubator for controlled sample processing and the Little Dipper Processor for FISH and G-Banding specimen preparation. SciGene also supplies FISH wash buffers and related reagent kits. The company serves clinical laboratories, research institutions, and pathology departments performing chromosomal analysis, genetic testing, and fluorescent probe-based diagnostic assays. Based in Santa Clara, California, SciGene operates as a direct supplier with an e-commerce platform, offering product ordering, order tracking, and customer service through phone and email. The company maintains business hours Monday–Friday, 9 AM–5 PM Pacific time, and commits to next-business-day response for customer inquiries.

Trademark Plastics Inc is a vertically integrated contract manufacturer specializing in precision plastic injection molding for the healthcare, pharmaceutical, diagnostics, and consumer products sectors. Founded in 1989, the company operates a 100,000 sq. ft. facility in Riverside, CA with 51 injection molding machines (6–610 ton capacity), 2 ISO Class 8 cleanrooms, and 2 controlled white rooms. TPI provides full turnkey solutions including plastic injection molding, rapid prototyping (5-day turnaround), mold design, tooling, and value-added services. Primary markets are medical device OEMs, IVD manufacturers, pharmaceutical companies, and diagnostic device makers. The company manufactures custom medical components, IVD supplies, lab supplies, and consumer products. TPI holds ISO 9001 and ISO 13485 certifications and operates in compliance with FDA regulations and MDR requirements, producing biocompatible and sterile-ready components. The company maintains operations in both the USA and China. Over 100 employees support design-for-manufacturability, precision tolerances, and lifecycle support for medical-grade plastic components.

Mawi DNA Technologies manufactures innovative biosample collection and stabilization devices for genomics, microbiome analysis, and molecular diagnostics. The company's flagship product line, iSWAB®, comprises proprietary swab-and-buffer systems designed to preserve DNA/RNA integrity while selectively controlling contamination. Key products include iSWAB-DNA (for human genomics with bacterial contamination suppression), iSWAB-RC-EL (FDA-cleared upper respiratory tract transport media suitable for extraction-less molecular testing), iSWAB-Microbiome (for microbiome sequencing and COVID-19 testing), iSWAB-Animal (for vertebrate DNA preservation in wildlife and zoological applications), and iSWAB-RNA. The company serves clinical laboratories, research institutions, forensic facilities, direct-to-consumer genomics companies, and animal science organizations. Products utilize non-toxic, proprietary lytic buffers that stabilize high molecular weight genomic DNA at variable temperatures and are suitable for infants through elderly populations. Mawi holds FDA clearance for select devices, CE marking for IVD use in EU markets, ISO 13485 certification, and UKCA approval. The company partners with genomics platforms, diagnostic test developers, and research institutions. Manufacturing and quality systems comply with medical device and research-grade standards.

GeminiBio is a biotechnology company founded in 1985, specializing in cell culture solutions and process liquids for the global biotechnology industry, with applications in cell and gene therapy, biotechnology research, and academic research. Operating from a 57,000 square-foot cGMP manufacturing facility in West Sacramento, California, the company is ISO 13485 certified and FDA registered as a Class 1 Medical Device Manufacturer. GeminiBio produces two core product categories: Cell Culture Solutions (including human serum AB, fetal bovine serum, and other animal sera) and Process Liquid Solutions (custom manufacturing of media, buffers, and high-purity water). The company offers Water for Injection (WFI) quality water, purified water, and custom buffer manufacturing in segregated animal origin-free and animal component facilities. Additionally, GeminiBio provides contract manufacturing and regulatory consulting services, emphasizing quality, transparency, and compliance with cGMP standards to support the discovery, development, and commercial production of transformative biotherapeutics.

Improve Medical USA, Inc. is a wholly-owned subsidiary of Improve Medical Instruments Co., Ltd. (ChiNext:300030), a publicly traded Chinese medical device manufacturer. The company operates as an authorized importer and full-service distributor of blood collection tubes, needle sets, and in vitro diagnostics (IVD) test products for the US clinical laboratory and nursing markets. Core product portfolio includes the IMPROVACUTER® line of blood collection tubes (EDTA and lithium heparin in standard and mini formats) and IMPROSAFE® multi-sample phlebotomy needles with integrated safety holders and blood collection sets. All products are FDA-registered and designed for preanalytical specimen collection and processing optimization. Beyond distribution, the company operates an OEM business providing custom manufacturing solutions for branded medical devices, maintains a BSL-2 laboratory in Carlsbad, California for research and development, and markets the Automatic Homogenization Processor for fecal specimen preparation. The company supports multiple business channels including direct distribution partnerships and a global distributor network. Target markets include clinical laboratories, hospitals, nursing facilities, and diagnostic service providers requiring high-quality preanalytical solutions. The company participates in industry conferences including Viticus Group WVC Annual Conference and PITTCON.

Lusis Biosciences is a California-based leader in qPCR assays and instruments for molecular diagnostics. The company specializes in VeraPoint qPCR assays and Q-Vera instruments designed for infectious disease detection across respiratory, urinary, sexually transmitted, gastrointestinal, and bloodborne pathogen applications. Lusis develops multiplexing technology-enabled reagents that simultaneously detect multiple targets, with a catalog of over 30 key products and hundreds of additional targets. The company also manufactures nucleic acid extraction reagents and sample processing solutions. Operating in over 160 countries with 10,000+ laboratory customers, Lusis combines integrated development and manufacturing capabilities with dedicated customer support and field application scientist consultation to deliver cost-effective, accessible molecular diagnostic solutions for clinical and research laboratories.

Liferiver Bio-Tech is a diagnostics company specializing in nucleic acid detection and molecular testing solutions. The company manufactures PCR-based diagnostic kits, automated extraction systems, and reagents for infectious disease detection across multiple pathogen categories including respiratory pathogens, sexually transmitted infections, hepatitis viruses, tumor markers, zoonotic diseases, and gastrointestinal pathogens. Primary product lines include the AutraMic mini4800 Plus automated workstation for nucleic acid extraction and PCR testing, ChinKing mini automation solution, and comprehensive real-time PCR kit portfolios. Liferiver's monkeypox detection kits are marketed for qualitative detection of monkeypox virus DNA in suspected cases. The company offers nucleic acid isolation kits (centrifuge column and AutoEX36 E variants), extraction consumables, and multiplex PCR reagents. Liferiver serves clinical laboratories and diagnostic centers globally, with product deployment across infectious disease surveillance, outbreak response, and routine patient testing. The company demonstrates regulatory compliance capabilities with product authentication support and regulatory documentation resources on their site. Manufacturing and distribution infrastructure supports both US/Canada markets and international territories, with animal-related products excluded from US sales per disclaimer.

IncellDx is a molecular diagnostics and biotechnology company specializing in single-cell diagnostics for precision medicine. The company develops and manufactures diagnostic tools, reagents, probes, and antibodies for multiplex RNA in situ hybridization and protein detection. Its proprietary SUSHI (Simultaneous Ultrasensitive Signal-amplified Hybridization In Situ) platform enables simultaneous analysis of proteomic and genomic biomarkers within intact cells without complex sample preparation. Key offerings include HPV OncoTect™ kits for cervical cancer detection, mRNA probes (HPV E6/E7, CMV), monoclonal antibodies (anti-PD-L1, anti-CD45, anti-Pan Cytokeratin), hybridization core reagents, fixatives, cell cycle assays, and the incellPREP™ tissue single-cell suspension system. Products are available in multiple regulatory statuses: RUO (Research Use Only), GPR (General Purpose Reagents), ASR (Analyte Specific Reagents), CE-IVD (European In Vitro Diagnostic), and US-IVD. The company holds FDA registration, EU IVD compliance certification, and ISO 13485 quality management certification. Clinical applications target serious viral diseases including cervical cancer, HIV/AIDS, hepatitis, COVID-19, and other malignancies.

IDS CO, LTD is a Japanese laboratory automation manufacturer headquartered in Kumamoto, Japan, specializing in specimen transport and automated sample handling systems for clinical laboratories worldwide. The company designs, manufactures, and maintains integrated specimen delivery and processing solutions that serve laboratories of all sizes and configurations. IDS products are manufactured entirely at the Kumamoto headquarters facility under a unified production system spanning development, design, manufacturing, software, sales, and maintenance—enabling consistent world-class quality control. The company maintains a significant global market share in laboratory automation, particularly in specimen transport system technology. Key product lines include the IDS-CLAS X-1 Series (next-generation specimen transport system), IDS-CLAS 3600 (front-end liquid handling/dispensing device), IDS-CLAS 2800 (front-end liquid handling/dispensing device), and IDS-Hr2 (fully automated urine dispensing system). IDS exhibits regularly at major international clinical laboratory conferences including JACLaS EXPO, ADLM (formerly AACC), and Euro MedLab, indicating strong market presence in Asia, North America, and Europe. The company emphasizes versatility and universal compatibility of its systems across diverse laboratory environments and workflows.

Fremon Scientific Inc manufactures ZipThaw®, a dry, portable, next-generation thawing device for cryopreserved blood products and cell therapy materials. The system uses patented temperature-monitoring technology with ZipSleeve® containment bags to achieve precise, uniform thawing without water baths. ZipThaw is designed for hospital blood banks, cell and gene therapy laboratories, bioproduction facilities, military medical settings, and veterinary clinics. The device offers approximately 50% faster thaw times compared to traditional water bath methods, eliminates cross-contamination risk, reduces product waste through on-demand thawing, requires minimal maintenance (warming cushion replacement every 2 years), and provides complete temperature documentation and audit trails. The company is veteran-owned and manufactures in the USA. ZipThaw holds FDA clearance, AABB compliance certification, CE marking, ISO certification, and UL listing. The system is trusted by military facilities including Fort Detrick, hospital blood banks, critical access hospitals, and cell therapy centers. Key advantages include dry operation (no water or toxic chemicals), compact footprint, user-friendly software with step-by-step guidance, spillage containment, and significant operational cost savings through elimination of water bath maintenance overhead.

Desco Industries Inc, established in 1979 (with origins dating to 1956 as Delta Electrical Specialty Company), is a diversified manufacturer and distributor of ESD control products and related industrial equipment for electronics manufacturing, cleanroom, and controlled-environment applications. The company operates under multiple brands including Desco, SCS, Menda, EDSYN, Tronex, Protektive Pak, Statguard Flooring, and EMIT. Core product offerings encompass ESD-protective equipment, wrist straps, worksurface and floor matting, component rework machines, static-shielding bags, ionizers, continuous monitors, testers, gloves, smocks, specialty tools, and workbench accessories. The company also manufactures non-ESD products including chemicals, grounding solutions, personnel identification systems, and material handling equipment. Manufacturing is primarily US-based with facilities in the United Kingdom and Japan. Desco maintains nine US inventory locations, two in the UK, one in Japan, and a sales office in Singapore. The company offers custom manufacturing to customer specifications and provides full technical and customer service support. Distribution occurs through a worldwide network of distributor partners. Desco holds ANSI-S20.20 training certification and provides ESD control training and technical guidance for electronics manufacturing environments.

Aiken Corporation is a Southern California-based laboratory equipment manufacturer founded in 1988. The company manufactures and exports a comprehensive range of general laboratory equipment using domestic and foreign components, serving hospitals and clinical laboratories in over 60 countries. Product lines include autoclaves, centrifuges, incubators, dry ovens, water and oil baths, biological safety cabinets, microscopes, tissue processors, balances, pH meters, conductivity meters, spectrophotometers, pipettes, refrigerators, and water purification systems. Additional offerings include microtomes, oscillators, polarimeters, clean benches, ultrasonic water baths, water distillers, and PRP (platelet-rich plasma) processing equipment. Aiken provides customer service Monday–Friday, 8:30 am–5 pm PST, including technical support, field service, maintenance, repair, and troubleshooting. The company emphasizes equipment reliability, operational performance, and total cost reduction for laboratory operations. Distribution is global, with manufacturing networks serving domestic and international markets.

Qvin develops non-invasive diagnostic solutions leveraging menstrual blood biomarkers for women's health screening and disease monitoring. The company's flagship product, the Q-Pad, is an FDA-cleared diagnostic menstrual pad that passively collects menstrual blood via an embedded Dried Menstrual Sample strip, enabling at-home collection of clinically valuable biospecimens without needles or invasive procedures. The Q-Pad has demonstrated strong clinical correlation with venous blood samples for biomarkers including HbA1c (r=0.96), TSH, and AMH (r>0.9), supporting its use in detecting and monitoring multiple conditions including diabetes, cervical cancer (HPV detection), endometriosis, sexually transmitted infections, and uterine fibroids. Qvin's research indicates menstrual effluent contains endometrial cells, immune components, hormones, and protein biomarkers reflective of both gynecological and systemic health, positioning it as an alternative to invasive biopsies, needle-based blood collection, and speculum-driven examinations such as Pap smears. The company partners with diagnostic platforms, healthcare organizations, and research institutions to expand the clinical validation and deployment of menstrual blood-based diagnostics. Qvin targets the women's health market, particularly addressing diagnostic access gaps in underserved populations. The company maintains an active research collaboration program with scientists, foundations, and non-profits to support clinical validation studies and innovation in period-blood diagnostics.

Total Source Manufacturing is a contract manufacturer and distributor of disposable apparel, cleanroom supplies, safety supplies, laboratory supplies, and medical supplies. Founded 25 years ago, the company operates ten distinct divisions, each with specialized product lines, serving medical, food handling, cleanroom, and industrial safety markets. The company manufactures and supplies a comprehensive range of personal protective equipment (PPE) including gloves (work gloves, disposable), finger cots, wipers, applicators, and cleanroom-specific items such as mats, tape, and electrostatic discharge control products. Additional offerings include lab supplies, cleaning supplies, and food service apparel. Total Source Manufacturing also offers private label manufacturing capabilities and maintains a distributor network. The company provides standardized product collections available in custom quantities, with 150+ product applications across 16 collections. Operations include multiple manufacturing facilities with global shipping capabilities, offering both pallet and full-container order fulfillment. Customer service includes fast order processing, tracking, and returns management. The company operates Monday–Friday, 8 AM–4 PM PST, with support via phone and email.

Bioneer Corporation is a life-science research supplier headquartered in Oakland, CA, specializing in molecular biology reagents, enzymes, nucleic acid synthesis and preparation kits, and laboratory instruments. The company manufactures and distributes a comprehensive portfolio including DNA/RNA amplification and prep reagents (AccuPrep kits for genomic DNA, mRNA, plant genomic DNA, and universal RNA), DNA/RNA synthesis reagents and phosphoramidites, polymerases and enzymes, oligonucleotides, RNAi products (siRNA and miRNA), gene synthesis services, protein expression and purification reagents, molecular markers and ladders, plastic consumables, and specialized instruments. Bioneer also offers drug target and toxicity identification services (GPScreen) and maintains a yeast genome-wide S. pombe knock-out library for functional genomics research. The company serves academic research institutions, biotechnology firms, pharmaceutical companies, and contract research organizations in North America. Products are supported by technical protocols, material safety data sheets, reference literature, and application notes. Bioneer maintains both US operations in Oakland and international headquarters in Daejeon, South Korea. The company provides customer support via toll-free phone, email, and direct technical assistance for product troubleshooting and applications development.

Biomiga, Inc. is a San Diego-based biotech research and manufacturing company specializing in nucleic acid extraction, purification, and PCR-based diagnostic products. Core product lines include the MgPure family of automated DNA/RNA extraction kits designed for diverse sample types: pathogenic, blood, saliva, circulating cell-free DNA, and formalin-fixed paraffin-embedded (FFPE) tissue. The company manufactures DNA/RNA size-selection beads offering superior yield (10–20% better than benchmarks) at competitive pricing, with full USA manufacturing and OEM customization capability. MgPure Seq DTR beads support sequencing workflows with >800 bp average reading lengths, available in manual or automated formats compatible with major platforms (Kingfisher Flex, Biomek, Hamilton, and others). Biomiga offers comprehensive real-time PCR detection assays targeting infectious disease panels, including respiratory pathogen panels (RPP), sexually transmitted infections (STI), gastrointestinal pathogens, women's health, wound infection markers, and nail fungal detection. The company also provides customized services for gene synthesis, cell line construction, protein expression, lentivirus packaging, and next-generation sequencing. FDA-registered facility with ISO 9001:2015 certification. All extraction protocols are fully validated for automation on industry-standard platforms. The company emphasizes in-house manufacturing control, 24/7 customer support, and R&D-driven product development.

Talladium is a B2B dental laboratory materials supplier and digital milling service provider based in Valencia, California. The company specializes in high-quality dental materials and CAD/CAM solutions for dental laboratories. Core product lines include One For All (OFA) Zirconia for restorative applications, TiLite medically pure dental alloys (FDA-cleared), investment materials, gypsum products, and custom refractory peg materials (Stick-It). Beyond materials supply, Talladium operates a full-service digital milling center (TMC) offering CAD/CAM milling services for dental technicians and labs seeking outsourced production capacity. The company emphasizes domestic manufacturing, quality control through university and FDA testing, and customer support including consulting and technical seminars to optimize laboratory workflows and efficiency.

Copan Group is a preanalytics and microbiology solutions provider founded in 1979, specializing in sample collection, transport systems, and diagnostic consumables for clinical laboratories, pharmaceutical, food, and personal care industries. The company manufactures proprietary sample collection and transport devices, including its flagship FLOQ® Technology for improved sample efficiency. Copan offers enrichment broths and culture media (including LBM® technology for selective cultivation such as Candida auris), molecular testing solutions (UBM™ non-toxic medium), and digital microbiology platforms. The company serves clinical labs with solutions for respiratory infections, antibiotic resistance testing, self-collection systems, clinical automation, and molecular biology applications. Copan also provides business alliances and custom collection devices for proprietary laboratory workflows. The company emphasizes quality certifications, regulatory compliance, R&D innovation through its "Science and R&D" program, and operates the CoScience HUB knowledge-sharing platform for microbiology excellence. Copan maintains ISO and quality compliance frameworks and participates in major scientific conferences (e.g., ESCMID). The organization pursues incubation and acceleration initiatives through its Futura Invent program.