Bioform Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Modification To Gfx Nerve Ablation System Ref K081729
Regimes: 510(k) Registry: 510(k)Radiesse Laryngeal Implant Ref K070090
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bioform Medical, Inc. have in the registry?
The registry currently lists 3 devices for Bioform Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bioform Medical, Inc.'s devices?
Among its 3 most recently registered devices, Bioform Medical, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Bioform Medical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Bioform Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bioform Medical, Inc. in the registry?
The most recently registered devices listed for Bioform Medical, Inc. include MODIFICATION TO GFX NERVE ABLATION SYSTEM, RADIESSE LARYNGEAL IMPLANT and JULIESSE INJECTABLE LARYNGEAL AUGMENTATION IMPLANT.