Evera Medical, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Evera Medical, Inc. makes
Evera Medical, Inc. manufactures facial reconstructive mesh (FRM) and orbital reconstructive implants, designed for surgical reconstruction in facial and orbital applications.
These devices are classified as Class II under FDA regulations and are listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Facial Reconstructive Mesh (Frm) Ref K063154
510(k) 510(k)Orbital Reconstructive Implant Ii Ref K083342
510(k) 510(k)
Frequently asked questions
How many devices does Evera Medical, Inc. have in the registry?
The registry currently lists 2 devices for Evera Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Evera Medical, Inc.'s devices?
Among its 2 most recently registered devices, Evera Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Evera Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Evera Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Evera Medical, Inc. in the registry?
The most recently registered devices listed for Evera Medical, Inc. include FACIAL RECONSTRUCTIVE MESH (FRM) and ORBITAL RECONSTRUCTIVE IMPLANT II.