Reselute
Also registered as Reselute, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3042025564
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Reselute Tibial Nail Ref K253517
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3042025564
- Address
- 701 W Main Street, Durham, NC, 27701
Frequently asked questions
How many devices does RESELUTE have in the registry?
The registry currently lists 1 device for RESELUTE. Devices recorded under merged duplicate company entries are counted once.
Which registries list RESELUTE's devices?
Among its 1 most recently registered device, RESELUTE has devices listed in FDA 510(k) (1 device).
What risk classes do RESELUTE's devices fall under?
Among its 1 most recently registered device, the classes recorded for RESELUTE's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from RESELUTE in the registry?
The most recently registered devices listed for RESELUTE include Reselute Tibial Nail.