Orthopedic Implants in Georgia

Unite Medical is a veteran-owned B2B wholesale medical supplies distributor serving healthcare professionals and providers nationwide. The company specializes in FDA-registered and ISO 13485-certified medical devices and consumables, offering member-only wholesale pricing with same-day shipping capabilities. Primary product lines include COVID, flu, and diagnostic test kits; N95 respirators and medical masks; and orthopedic bracing solutions. All products meet regulatory standards and are sourced from ISO 13485-certified manufacturers. Beyond distribution, Unite Medical provides consulting services for product commercialization, including CMS/PDAC credential acquisition and private-label manufacturing support to help healthcare companies bring products to market. The company emphasizes fast order processing, secure checkout, and expert guidance for healthcare procurement professionals.

Poriferous LLC is a medical device manufacturer specializing in advanced porous polyethylene surgical implants for craniomaxillofacial reconstruction and augmentation. The company develops and distributes SU-POR®, a proprietary line of biocompatible implants featuring an interconnecting, omnidirectional pore structure designed to promote fibrovascular ingrowth and tissue integration. Product categories include cranial implants for skull and bone defect repair, orbital implants for eye socket reconstruction, facial implants for aesthetic and reconstructive augmentation, and patient-specific custom implants tailored to individual surgical requirements. SU-POR implants are manufactured from premium porous polyethylene, are non-pyrogenic, MR Safe, EO sterilized, and available in ready-to-use or customizable configurations. The company serves surgeons, patients, and international distributors, emphasizing clinical reliability, biocompatibility, durability, and ease of surgical modification. Products are designed with surgeon feedback and clinical expertise to support secure tissue integration and long-term stability. Poriferous markets its implants globally through a distributor network and directly to surgical specialists in craniomaxillofacial, reconstructive, and aesthetic surgery.

Matrix Surgical USA designs, manufactures, and distributes OMNIPORE® porous high-density polyethylene implants for craniofacial reconstructive and aesthetic surgery. The company specializes in both standard surgical implants and customized patient-specific implants using advanced computer imaging and 3D modeling technologies. Product lines include facial augmentation implants (chin, malar, rim, midface, mandibular), neurosurgical implants for cranial and skull-based reconstruction, reconstructive shapes for traumatic defects and microtic ear reconstruction, orbital trauma correction implants (sheets, wedges, blocks), and spheres for enucleation and evisceration procedures. OMNIPORE implants have received FDA 510(k) clearance, CE marking in Europe, and regulatory approvals from ANVISA (Brazil), KFDA (South Korea), TFDA (Taiwan), TGA (Australia), and other stringent regulatory authorities. Manufacturing is performed in the USA to meet quality and reliability standards. The company serves plastic surgeons, otolaryngologists, neurosurgeons, and oral maxillofacial surgeons globally. Matrix Surgical USA operates with a subsidiary presence in Brazil as of 2024, expanding its international distribution and market reach in Latin America.

SPS (Symbiont Logistics, LLC) is a leading distributor of orthotic and prosthetic (O&P) products in the United States, supplying over 400,000 items to healthcare professionals and clinicians. The company specializes in prosthetics, orthotics, footwear, compression garments, and fabrication supplies from top manufacturers including Aspen Medical Products and other industry leaders. SPS maintains a comprehensive inventory of PDAC-approved products across multiple L-codes (L5987, L5981, L5980, L5973, L5857, L5856) to support diverse clinical needs. Beyond product distribution, SPS Clinical Services delivers training and continuing education programs on product selection, fitting, and clinical applications through in-person and digital channels. The company's experienced clinical team provides practitioners with insights and education to support improved patient outcomes. SPS is committed to enabling healthcare providers to adapt to evolving technology and policy requirements while freeing clinicians to prioritize direct patient care.

MiRus is a medical device company developing proprietary implants and procedural solutions leveraging its proprietary Molybdenum-Rhenium (MoRe®) alloy technology. The company focuses on cardiovascular and orthopedic applications with an integrated platform spanning pre-operative, intra-operative, and post-operative solutions. MiRus' core technology, MoRe®, represents over 15 years of R&D and offers advantages over traditional medical materials (titanium, cobalt chromium) including smaller implant profiles, improved durability, enhanced biocompatibility, and significantly lower metal ion release. The company's cardiovascular portfolio includes the Siegel™ Transcatheter Aortic Valve (TAVR) system, currently in the STAR randomized controlled trial for symptomatic severe aortic stenosis. The orthopedic portfolio includes the IO™ Expandable Wedge Osteotomy System (FDA 510(k) cleared February 2026) and the EUROPA™ Posterior Cervical Fusion System (recipient of FDA New Technology Add-on Payment, NTAP). MiRus is headquartered in Marietta, Georgia, and was founded by experienced entrepreneurs with a track record of developing disruptive medical technologies. The company maintains an active clinical development program with multi-center trials and regulatory engagement with the FDA.

Bodycad is a precision orthopedic solutions provider specializing in patient-specific deformity correction through advanced 3D imaging and personalized surgical planning. The company's proprietary Personalized Restoration™ technology enables orthopedic surgeons to customize surgical procedures to each patient's unique anatomy. Bodycad's flagship offering, Fine Osteotomy™, is an end-to-end solution combining 3D image planning, patent-pending drill-stop cutting technology, and personalized plating systems. The platform delivers customized surgical guides and patient-specific implants designed for precise bone deformity correction procedures, including lateral open wedge distal femoral osteotomy and similar corrections. The company operates a clinical design service model where surgeons schedule consultations, submit CT and X-ray imaging via the Preplink platform, and receive tailored surgical kits within defined timelines. Bodycad has performed over 2,000 orthopedic procedures and serves 500+ orthopedic surgeons. The company distributes through partner networks and maintains a distribution program. Based on press releases, Bodycad is headquartered in Québec, Canada, with US operations. Manufacturing and clinical design capabilities support FDA-regulated custom implant production, though specific regulatory certifications were not detailed on the visible homepage content.

AAP IMPLANTATE AG is a German orthopedic trauma implant manufacturer specializing in fracture fixation plates and screws. The company develops and manufactures the LOQTEQ® product line, a patented locking compression plate platform technology that combines fracture compression with angular-stable locking in a single operative step. The LOQTEQ® portfolio covers over 95% of relevant trauma indications in upper and lower extremity fracture treatment, including distal tibia and fibula plates, with applications in ankle injuries, sports medicine, and general traumatology. AAP is a pure-play trauma specialist focused on addressing unmet clinical needs through innovative implant technologies. The company offers three core technology platforms: LOQTEQ® standard locking compression plates in titanium (designed to minimize cold-weld effects), LOQTEQ® antibacterial implants featuring silver-coating technology to reduce implant-related infections, and LOQTEQ® resorbable implants using magnesium with hydroxyapatite coating that bioresorb post-fracture healing, eliminating the need for removal surgery. Manufacturing is conducted in Germany. Products carry CE marking, FDA 510(k) clearance, NMPA, and ANVISA approvals. The company markets to trauma surgeons, orthopedic hospitals, and surgical centers globally, with demonstrated clinical success in professional and amateur sports medicine contexts.

OrthoCircle is a Savannah, Georgia-based surgical instrument distributor specializing in premium orthopedic surgical instruments and cutting tools. As the exclusive U.S.-based distributor of Komet Medical products, OrthoCircle provides German-engineered orthopedic fixation devices, including orthopedic pins, saw blades, drill bits, and rotary burrs. The company serves surgical teams requiring advanced instruments for orthopedic procedures at competitive pricing. OrthoCircle also offers contract manufacturing and sterile packaging services through its Komet Medical partnership, enabling customized solutions for surgical instrument procurement and supply chain optimization.

Southern Spine, LLC manufactures spinal fixation and fusion implants for minimally invasive spine surgery (MIS). The company's product portfolio includes the StabiLink® MIS Spinal Fixation System (featuring patented Laminar Lock design for L4-L5 and L5-S1 applications), Kwik-Fix® interbody fusion devices, and C-Fuse® cervical fusion implants. Southern Spine serves orthopedic and neurosurgical institutions with instruments and implants designed for posterior and interbody fusion procedures, including pediatric applications. The company has demonstrated regulatory and clinical credibility, having won Medical Design Excellence awards (2015) and presenting clinical case data and instructional videos for surgeon training. Products are marketed to spine surgery centers and hospital operating rooms. Manufacturing and regulatory certifications are not explicitly detailed on the homepage, but the company's established product line and clinical support infrastructure indicate FDA clearance or 510(k) approval for spinal implant categories.

Arrowhead DE LLC manufactures the ARROW-LOK Digital Fusion System, an innovative fixation device designed for proximal interphalangeal (PIP) joint fusion in foot and ankle surgery. The system provides enhanced rotational stability and resistance to migration compared to traditional Kirschner wire (K-wire) fixation, which has been the standard for over 40 years. The ARROW-LOK implant features a 3-dimensional arrow design with biocompatible material properties and a simplified operative technique that reduces post-operative management complexity for patients. The device is engineered as an alternative to smooth 1.1mm or 1.6mm K-wires, targeting progressive foot and ankle specialists who seek improved fixation stability. The company positions the system as simple, easy, and effective for providing enhanced care in digital joint fusion procedures.