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Porex Surgical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
19
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K102184MEDPOR CONTAIN CAN IMPLANTJanuary 7, 2011
K101835MEDPOR FIXATION SYSTEM-CRANIAL, MODELS 80080, 80079December 3, 2010
K091807MEDPOR FIXATION SYSTEMJune 28, 2010
K091120MEDPOR CONTAIN IMPLANTMarch 19, 2010
K083621MEDPOR CUSTOMIZED SURGICAL IMPLANTFebruary 3, 2009
K071335MEDPOR ATTRACTOR IMPLANTAugust 8, 2007
K052297POREX ELECTROSURGERY NEEDLEMarch 28, 2006
K040851MEDPOR ATTRACTOR MAGNETIC COUPLING SYSTEMJuly 16, 2004
K040364MEDPOR CRANIOFACIAL IMPLANTS WITH EMBEDDED TITANIUM MESHJune 30, 2004
K021357MEDPOR PLUS ORBITAL VOLUME REPLACEMENT IMPANTAugust 5, 2002
K012350MEDPOR PLUS SURGICAL IMPLANT BIOMATERIALMarch 14, 2002
K012108MEDPOR COATED TEAR DRAINDecember 19, 2001
K010902MEDPOR QUAD MOTILITY IMPLANTJune 19, 2001
K982040MEDPOR SURGICAL GRANULE IMPLANTSSeptember 8, 1998
K981374POREX NOSTRIL RETAINERSJuly 2, 1998
K972034MEDPOR OCULAR CONFORMERJanuary 20, 1998
K954939MEDPOR OCULAR SCREW & ACCESSORIESJanuary 25, 1996
K952677MEDPOR BARRIER SURGICAL IMPLANT BIOMATERIALAugust 21, 1995
K943275MEDPOR SURGICAL IMPLANT MATERIALSeptember 2, 1994