Bridger Biomed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bridger Biomed, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Bridger Biomed, Inc. has 7 FDA 510(k) cleared medical devices. Based in Bozeman, US.
Historical record: 7 cleared submissions from 1997 to 2001. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Bridger Biomed, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bridger Biomed, Inc.
7 devices
Cleared
Jan 26, 2001
MODIFICATION TO FLUROTEX SURGICAL MESH
General & Plastic Surgery
38d
Cleared
Jan 26, 2001
MODIFICATION TO FLUOROTEX II SURGICAL MESH
General & Plastic Surgery
38d
Cleared
Aug 26, 2000
FLUOROTEX II SURGICAL MESH
General & Plastic Surgery
24d
Cleared
Jul 07, 2000
FLUORO-TEX CARDIOVASCULAR PATCH
Cardiovascular
224d
Cleared
Jan 07, 1999
FLUOROTEX SURGICAL MESH
General & Plastic Surgery
45d
Cleared
May 13, 1998
DURA-PATCH MODEL DP-XXX
Neurology
90d
Cleared
Nov 24, 1997
FLUORO-TEX SURGICAL MEMBRANE
Cardiovascular
91d