Nebl, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Nebl, Inc. makes
Nebl, Inc. manufactures medical devices including the RESTORE (also known as RE/STOR and CAPSURE) and the CAP-AID, which are designed for orthopedic applications, such as joint preservation and cartilage restoration procedures.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Restore (Aka Re/Stor) Ref K983164
Regimes: 510(k) Registry: 510(k)Cap-Aid Ref K954959
Regimes: 510(k) Registry: 510(k)Restore (A.K.A. Capsure) Ref K971359
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nebl, Inc. have in the registry?
The registry currently lists 3 devices for Nebl, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nebl, Inc.'s devices?
Among its 3 most recently registered devices, Nebl, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Nebl, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Nebl, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Nebl, Inc. in the registry?
The most recently registered devices listed for Nebl, Inc. include RESTORE (AKA RE/STOR), CAP-AID and RESTORE (A.K.A. CAPSURE).