Metagen, LLC
United StatesFDA applicant, unverified
- Devices
- 5
What Metagen, LLC makes
Metagen, LLC manufactures orthopedic implants and surgical systems for lower-limb and hip reconstruction, including modular femoral hip systems, acetabular cup replacements, wire cerclage systems for bone stabilization, high tibial osteotomy tools, and segmental defect replacement components.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Activelock Modular Femoral Hip System Ref K980020
Regimes: 510(k) Registry: 510(k)Metagen All Poly Acetabular Cup System Ref K964003
Regimes: 510(k) Registry: 510(k)Metagen Activelock Wire Cerclage System Ref K983976
Regimes: 510(k) Registry: 510(k)Metagen High Tibial Osteotomy System Ref K963700
Regimes: 510(k) Registry: 510(k)Segmental Defect Replacement System Ref K980609
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Metagen, LLC have in the registry?
The registry currently lists 5 devices for Metagen, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Metagen, LLC's devices?
Among its 5 most recently registered devices, Metagen, LLC has devices listed in FDA 510(k) (5 devices).
What risk classes do Metagen, LLC's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Metagen, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Metagen, LLC in the registry?
The most recently registered devices listed for Metagen, LLC include ACTIVELOCK MODULAR FEMORAL HIP SYSTEM, METAGEN ALL POLY ACETABULAR CUP SYSTEM, METAGEN ACTIVELOCK WIRE CERCLAGE SYSTEM and METAGEN HIGH TIBIAL OSTEOTOMY SYSTEM.