Biomet Trauma
Country not established
- Devices
- 7
What Biomet Trauma makes
Biomet Trauma manufactures orthopedic trauma devices including the OPTILOCK PERIARTICULAR PLATING, BIODRIVE CANNULATED SCREW SYSTEM, LOWER EXTREMITY EXTERNAL FIXATION - EXPANDED INDICATIONS, BIOMET VARIABLE LOCKING PLATE SYSTEM, BIOMET PHOENIX ANKLE NAIL AND ANKLE ARTHRODESIS NAIL, GROWTH CONTROL PLATING SYSTEM, and BIOMET PHOENIX ANKLE NAIL SYSTEM.
The company's devices are Class II and listed in the FDA 510(k) registry. Biomet Trauma is based in the US.
Catalogue
Optilock Periarticular Plating Ref K092078
Regimes: 510(k) Registry: 510(k)Biodrive Cannulated Screw System Ref K082874
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Biomet Variable Locking Plate System Ref K071325
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Growth Control Plating System Ref K070823
Regimes: 510(k) Registry: 510(k)Biomet Phoenix Ankle Nail System Ref K081243
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biomet Trauma have in the registry?
The registry currently lists 7 devices for Biomet Trauma. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biomet Trauma's devices?
Among its 7 most recently registered devices, Biomet Trauma has devices listed in FDA 510(k) (7 devices).
What risk classes do Biomet Trauma's devices fall under?
Among its 7 most recently registered devices, the classes recorded for Biomet Trauma's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biomet Trauma in the registry?
The most recently registered devices listed for Biomet Trauma include OPTILOCK PERIARTICULAR PLATING, BIODRIVE CANNULATED SCREW SYSTEM, LOWER EXTREMITY EXTERNAL FIXATION - EXPANDED INDICATIONS and BIOMET VARIABLE LOCKING PLATE SYSTEM.