Biomerix Corporation - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Biomerix Corporation General & Plastic Surgery ✕
5 devices
Cleared
Dec 23, 2011
BIOMERIX COMPOSITE SURGICAL MESH
General & Plastic Surgery
115d
Cleared
Dec 23, 2011
BIOMERIX ASSURE
General & Plastic Surgery
112d
Cleared
May 13, 2010
BIOMERIX VENTRAL HERNIA REPAIR MESH, MODEL SM3-TAB
General & Plastic Surgery
223d
Cleared
Jan 07, 2009
BIOMERIX COMPOSITE SURGICAL MESH, MODEL SMNR-0510 AND SMNR-1215
General & Plastic Surgery
97d
Cleared
Feb 25, 2008
BIOMERIX SURGICAL MESH, MODEL: RCR-01
General & Plastic Surgery
326d