Porex Surgical, Inc. is one of 15029 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Porex Surgical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MEDPOR CONTAIN CAN IMPLANT, MEDPOR FIXATION SYSTEM-CRANIAL, MODELS 80080, 80079, MEDPOR FIXATION SYSTEM
19
Total
19
Cleared
0
Denied
Porex Surgical, Inc. has 19 FDA 510(k) cleared medical devices. Based in Fairburn, US.
Historical record: 19 cleared submissions from 1994 to 2011. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Porex Surgical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Porex Surgical, Inc.
19 devices
Cleared
Jan 07, 2011
MEDPOR CONTAIN CAN IMPLANT
Dental
158d
Cleared
Dec 03, 2010
MEDPOR FIXATION SYSTEM-CRANIAL, MODELS 80080, 80079
Neurology
155d
Cleared
Jun 28, 2010
MEDPOR FIXATION SYSTEM
Dental
375d
Cleared
Mar 19, 2010
MEDPOR CONTAIN IMPLANT
Dental
336d
Cleared
Feb 03, 2009
MEDPOR CUSTOMIZED SURGICAL IMPLANT
Ear, Nose, Throat
57d
Cleared
Aug 08, 2007
MEDPOR ATTRACTOR IMPLANT
Ophthalmic
89d
Cleared
Mar 28, 2006
POREX ELECTROSURGERY NEEDLE
General & Plastic Surgery
217d
Cleared
Jul 16, 2004
MEDPOR ATTRACTOR MAGNETIC COUPLING SYSTEM
Ophthalmic
107d
Cleared
Jun 30, 2004
MEDPOR CRANIOFACIAL IMPLANTS WITH EMBEDDED TITANIUM MESH
General & Plastic Surgery
138d
Cleared
Aug 05, 2002
MEDPOR PLUS ORBITAL VOLUME REPLACEMENT IMPANT
Ophthalmic
98d
Cleared
Mar 14, 2002
MEDPOR PLUS SURGICAL IMPLANT BIOMATERIAL
General & Plastic Surgery
232d
Cleared
Dec 19, 2001
MEDPOR COATED TEAR DRAIN
Ophthalmic
166d