Medical Device Manufacturer · US , Rockville , MD

Biomerix Corporation - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2005

Recent clearances: BIOMERIX COMPOSITE SURGICAL MESH, BIOMERIX ASSURE, BIOMERIX VENTRAL HERNIA REPAIR MESH, MODEL SM3-TAB

View 6 510(k) Devices ↓
6
Total
6
Cleared
0
Denied

FDA 510(k) Regulatory Record - Biomerix Corporation General & Plastic Surgery ✕

5 devices
1-5 of 5
Cleared Dec 23, 2011
BIOMERIX COMPOSITE SURGICAL MESH
K112499 · FTL
General & Plastic Surgery · 115d
Cleared Dec 23, 2011
BIOMERIX ASSURE
K112567 · FTL
General & Plastic Surgery · 112d
Cleared May 13, 2010
BIOMERIX VENTRAL HERNIA REPAIR MESH, MODEL SM3-TAB
K093123 · FTL
General & Plastic Surgery · 223d
Cleared Jan 07, 2009
BIOMERIX COMPOSITE SURGICAL MESH, MODEL SMNR-0510 AND SMNR-1215
K082941 · FTL
General & Plastic Surgery · 97d
Cleared Feb 25, 2008
BIOMERIX SURGICAL MESH, MODEL: RCR-01
K070961 · FTL
General & Plastic Surgery · 326d
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