Brennen Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Brennen Medical, Inc. - FDA 510(k) Cleared Devices
17
Total
16
Cleared
0
Denied
Brennen Medical, Inc. has 16 FDA 510(k) cleared general & plastic surgery devices. Based in St, Paul, US.
Historical record: 16 cleared submissions from 1994 to 2006.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Brennen Medical, Inc.
17 devices
Cleared
Feb 17, 2006
BRENNEN MEDICAL SILVER GLUCAN WOUND DRESSING
General & Plastic Surgery
400d
Cleared
Mar 07, 2003
MODIFICATION TO BRENNEN BIOSYNTHETIC SURGICAL MESH MATRIX
Gastroenterology & Urology
23d
Cleared
Oct 17, 2002
BRENNEN MEDICAL SURGICAL MESH, GLUCAMESH/GLUCATEX
General & Plastic Surgery
135d
Cleared
Oct 02, 2000
GLUCANPRO CREAM
General & Plastic Surgery
84d
Cleared
Oct 02, 2000
BETA GLUCAN GEL (MACROPRO GEL)
General & Plastic Surgery
84d
Cleared
May 01, 2000
MACROPRO GEL
General & Plastic Surgery
75d
Cleared
May 01, 2000
GLUCANPRO
General & Plastic Surgery
75d
Cleared
Nov 06, 1998
BRENNEN MEDICAL BETA GLUCAN GEL
General & Plastic Surgery
87d
Cleared
Sep 22, 1998
BRENNEN BIOSYNTHETIC SURGICAL MESH MATRIX
Gastroenterology & Urology
74d
Cleared
Jul 29, 1998
BRENNEN MEDICAL BETA GLUCAN CREAM, MACROPRO
General & Plastic Surgery
135d
Cleared
Dec 12, 1996
BRENNEN MEDICAL GLUCAN II WOUND DRESSING
General & Plastic Surgery
49d
Cleared
Dec 05, 1996
NOVAGEL SILICONE GEL SHEETING
General & Plastic Surgery
115d