Brennen Medical, Inc.
Brennen Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2006.
Top product codes for Brennen Medical, Inc.
Recent clearances by Brennen Medical, Inc.
- K050086 — BRENNEN MEDICAL SILVER GLUCAN WOUND DRESSING
- K030460 — MODIFICATION TO BRENNEN BIOSYNTHETIC SURGICAL MESH MATRIX
- K021835 — BRENNEN MEDICAL SURGICAL MESH, GLUCAMESH/GLUCATEX
- K002077 — GLUCANPRO CREAM
- K002078 — BETA GLUCAN GEL (MACROPRO GEL)
- K000518 — MACROPRO GEL
- K000519 — GLUCANPRO
- K982825 — BRENNEN MEDICAL BETA GLUCAN GEL
- K982403 — BRENNEN BIOSYNTHETIC SURGICAL MESH MATRIX
- K980962 — BRENNEN MEDICAL BETA GLUCAN CREAM, MACROPRO
- K964241 — BRENNEN MEDICAL GLUCAN II WOUND DRESSING
- K963128 — NOVAGEL SILICONE GEL SHEETING
- K950032 — MEDISKIN(R) SS, ZENODERM BIOLOGICAL WOUND DRESSING
- K950281 — MESH MATRIX WOUND DRESSING
- K935189 — E-Z DERM BIOSYNTHETIC WOUND DRESSING
- K941125 — NOVAGEL SILICONE GEL SHEETING
- K935060 — BRENNEN MEDICAL STERILE SALINE SOLUTION
Data sourced from openFDA. This site is unofficial and independent of the FDA.