Osteo AG
Country not established
- Devices
- 9
What Osteo AG makes
Osteo AG manufactures orthopedic fixation devices including external fixators, Kirschner wires, compression hip screws, interlocking-compression nails, femoral nails, pneumatic drills, cerclage wires, tibia nails, and Steinmann pins.
These devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Osteo Ex-Fi-Re Ref K920149
Regimes: 510(k) Registry: 510(k)Osteo Kirschner Wire Ref K922193
Regimes: 510(k) Registry: 510(k)Osteo Compression Hip Screw Ref K920037
Regimes: 510(k) Registry: 510(k)Osteo Interlocking-Compression Nail Ref K933340
Regimes: 510(k) Registry: 510(k)Osteo Femoral Nail Ref K922195
Regimes: 510(k) Registry: 510(k)Osteo Complete Pneumatic Drill-Oscilair Ref K913559
Regimes: 510(k) Registry: 510(k)Osteo Cerclage Wire Ref K914374
Regimes: 510(k) Registry: 510(k)Osteo Tibia Nail Ref K922196
Regimes: 510(k) Registry: 510(k)Osteo Steinmann Pin Ref K922194
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Osteo AG have in the registry?
The registry currently lists 9 devices for Osteo AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Osteo AG's devices?
Among its 9 most recently registered devices, Osteo AG has devices listed in FDA 510(k) (9 devices).
What risk classes do Osteo AG's devices fall under?
Among its 9 most recently registered devices, the classes recorded for Osteo AG's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Osteo AG in the registry?
The most recently registered devices listed for Osteo AG include OSTEO EX-FI-RE, OSTEO KIRSCHNER WIRE, OSTEO COMPRESSION HIP SCREW and OSTEO INTERLOCKING-COMPRESSION NAIL.