Porex Surgical, Inc. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
FDA 510(k) Regulatory Record - Porex Surgical, Inc. General & Plastic Surgery ✕
4 devices
Cleared
Mar 28, 2006
POREX ELECTROSURGERY NEEDLE
General & Plastic Surgery
217d
Cleared
Jun 30, 2004
MEDPOR CRANIOFACIAL IMPLANTS WITH EMBEDDED TITANIUM MESH
General & Plastic Surgery
138d
Cleared
Mar 14, 2002
MEDPOR PLUS SURGICAL IMPLANT BIOMATERIAL
General & Plastic Surgery
232d
Cleared
Aug 21, 1995
MEDPOR BARRIER SURGICAL IMPLANT BIOMATERIAL
General & Plastic Surgery
70d