Porex Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Porex Medical - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Porex Medical has 15 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.
Historical record: 15 cleared submissions from 1983 to 1987.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Porex Medical
15 devices
Cleared
Oct 20, 1987
POREX NERVE LOCATOR
Ear, Nose, Throat
98d
Cleared
Sep 04, 1987
POREX OTOLOGY INSTRUMENTS
Ear, Nose, Throat
31d
Cleared
Aug 21, 1987
POREX QUALITY PLASTIC SURGERY INSTRUMENTS
General & Plastic Surgery
24d
Cleared
Feb 27, 1987
POREX(TM) EYE SPHERE IMPLANT
Ophthalmic
140d
Cleared
Feb 27, 1987
POREX(TM) EXTRA-OCULAR ORBITAL IMPLANT
Ophthalmic
140d
Cleared
Feb 24, 1987
POREX(TM) TISSUE EXPANDER
General & Plastic Surgery
42d
Cleared
Feb 24, 1987
POREX(TM) MALAR IMPLANT
General & Plastic Surgery
39d
Cleared
Feb 24, 1987
POREX(TM) SILICONE SURGICAL IMPLANTS FOR E.N.T.
General & Plastic Surgery
32d
Cleared
Oct 24, 1986
POREX(TM) EAR PROSTHESIS
General & Plastic Surgery
14d
Cleared
Oct 24, 1986
POREX(TM) PROSTHESIS, CHIN, INTERNAL
General & Plastic Surgery
14d
Cleared
Oct 24, 1986
POREX(TM) NOSE PROSTHESIS
General & Plastic Surgery
14d
Cleared
Mar 13, 1986
THE POREX RETRACTOR TABLE
General & Plastic Surgery
30d