Implanet
FranceFDA applicant, unverified FDA FEI 3007675554
- Devices
- 1,169
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Implanet makes
Implanet manufactures spinal fixation devices, including trans-facet screws, internal fixation rods, polymeric interbody fusion cages, and cable tensioners for spinal stabilization. Their portfolio also includes cruciate-retaining total knee prostheses, orthopaedic surgical kits, and reusable instrument trays for orthopaedic procedures.
The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Implanet is based in the United States.
Catalogue
Search and filter all 1,169 devicesShowing 1-50 of 1,169
Company details
- FDA FEI number
- 3007675554
- DUNS number
- 291993439
- Address
- Technopole Bordeaux Montesquieu, Martillac Nouvelle-Aquitaine
Frequently asked questions
How many devices does Implanet have in the registry?
The registry currently lists 1169 devices for Implanet. Devices recorded under merged duplicate company entries are counted once.
Which registries list Implanet's devices?
Among its 50 most recently registered devices, Implanet has devices listed in FDA GUDID (50 devices).
What risk classes do Implanet's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Implanet's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Implanet in the registry?
The most recently registered devices listed for Implanet include Jazz Spinal System 570075, Jazz Spinal System 570083, Jazz Spinal System 631049 and Jazz Spinal System 631054.