Maintenance & Repair in Wisconsin

MedDev is a healthcare technology company specializing in regenerative medicine and advanced wound care solutions. The company distributes biologic skin substitutes based on amniotic membrane technology, designed to accelerate healing in chronic wounds, burn wounds, ophthalmic applications, and surgical procedures. Their product portfolio includes multiple branded skin substitute lines (XCell, XCellerate, Royal Wound, Precise, Royal Bio, BioLab, DermMax, and EnColl). Beyond product distribution, MedDev provides integrated practice optimization services including revenue cycle management, workflow efficiency enhancement, administrative burden reduction, and scheduling optimization. The company serves healthcare providers, clinical partners, and distributors across the United States. MedDev's regenerative solutions leverage amniotic membrane grafts containing growth factors and cytokines to promote cell proliferation, tissue regeneration, inflammatory modulation, and minimal immune response. The company emphasizes compliance-first operations, clinical research backing, and hands-on provider support. Their business model combines premium biologic products with comprehensive practice management services to optimize both patient outcomes and provider operations.

Wisconsin Pharmacal Co., LLC is a full-service contract manufacturer and private-label producer with over 125 years of industry experience. The company specializes in comprehensive manufacturing solutions for OTC drugs, cosmetics, medical devices, personal care, first-aid, and household products. Core manufacturing capabilities include liquids (hot/cold formulation), lotions and creams, gels, ointments, suppositories, lubricants, foams, washes, sterilized saline, and shampoo formulations. Packaging services encompass bottles, tubes, blister carding, over-wraps, cartons, jars, and bag-on-valve (BOV) systems. The facility operates under FDA and EPA compliance with GMP certification and UL-certified management systems compliant with 21 CFR Part 820 (medical devices) and 21 CFR Parts 210/211 (OTC drugs). On-site capabilities include a dedicated microbiology and analytical chemistry laboratory staffed by an experienced R&D team supporting custom product development, regulatory compliance, raw material sourcing, validation, and commercial-scale production. The company serves the personal care, skin care, bath care, hair care, feminine hygiene, medical device, and OTC pharmaceutical sectors with flexible minimum order quantities and documented 95%+ on-time, in-full delivery performance. Pharmacal maintains an ACLASS Accredited Inspection Body designation and is Thomas-verified as a supplier.

Dedicated Computing is a Wisconsin-based original design manufacturer (ODM) founded in 1978, specializing in the design, development, and manufacturing of embedded computing systems, hardware, and software platforms for OEMs in mission-critical industries. The company delivers high-performance, reliable, and customizable solutions for healthcare, training and simulation, and industrial automation. Dedicated Computing manufactures complete, certified, integrated systems optimized for OEM applications, including custom computing platforms, rack-scale integration, and comprehensive lifecycle management services. The company powers essential medical devices and professional training simulators, and partners with leading technology firms including Intel, NVIDIA, and AMD. Its DC Digital Services offering includes proactive system lifecycle management, component obsolescence planning, embedded OS transitions, remote diagnostics, and 24/7 support services. Dedicated Computing emphasizes quality, reliability, and compliance in high-stakes environments.

MAK and Associates is a regulatory compliance and quality consulting firm specializing in medical device regulatory support. Led by Steve Krueger, a computer engineer and Six Sigma Black Belt with 20+ years of medical device industry experience, the firm provides expert guidance in FDA compliance, verification and validation, quality systems development, post-market surveillance, adverse event reporting, and regulatory submissions. Services include US FDA Agent representation for international medical device companies, compliance monitoring programs, and risk-based testing strategies. The firm serves medical device startups and established manufacturers navigating FDA, MDR, and ISO requirements to accelerate market entry and ensure regulatory compliance.