Bridger Biomed, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 7
What Bridger Biomed, Inc. makes
Bridger Biomed, Inc. manufactures surgical meshes and membranes, including Fluorotex and Fluorotex II variants for hernia repair and related procedures, as well as cardiovascular patches and dura patches for neurological applications.
These products are classified as Class II devices under FDA regulations and are authorised via the 510(k) pathway. The company operates from the United States.
Catalogue
Fluorotex Surgical Mesh Ref K984197
510(k) 510(k)Modification To Flurotex Surgical Mesh Ref K003906
510(k) 510(k)Modification To Fluorotex Ii Surgical Mesh Ref K003917
510(k) 510(k)Fluoro-Tex Surgical Membrane Ref K973178
510(k) 510(k)Fluorotex Ii Surgical Mesh Ref K002351
510(k) 510(k)Fluoro-Tex Cardiovascular Patch Ref K994032
510(k) 510(k)Dura-Patch Model Dp-Xxx Ref K980548
510(k) 510(k)
Frequently asked questions
How many devices does Bridger Biomed, Inc. have in the registry?
The registry currently lists 7 devices for Bridger Biomed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bridger Biomed, Inc.'s devices?
Among its 7 most recently registered devices, Bridger Biomed, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Bridger Biomed, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Bridger Biomed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bridger Biomed, Inc. in the registry?
The most recently registered devices listed for Bridger Biomed, Inc. include FLUOROTEX SURGICAL MESH, MODIFICATION TO FLUROTEX SURGICAL MESH, MODIFICATION TO FLUOROTEX II SURGICAL MESH and FLUORO-TEX SURGICAL MEMBRANE.