Porex Surgical, Inc.
Porex Surgical, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2011.
Top product codes for Porex Surgical, Inc.
Recent clearances by Porex Surgical, Inc.
- K102184 — MEDPOR CONTAIN CAN IMPLANT
- K101835 — MEDPOR FIXATION SYSTEM-CRANIAL, MODELS 80080, 80079
- K091807 — MEDPOR FIXATION SYSTEM
- K091120 — MEDPOR CONTAIN IMPLANT
- K083621 — MEDPOR CUSTOMIZED SURGICAL IMPLANT
- K071335 — MEDPOR ATTRACTOR IMPLANT
- K052297 — POREX ELECTROSURGERY NEEDLE
- K040851 — MEDPOR ATTRACTOR MAGNETIC COUPLING SYSTEM
- K040364 — MEDPOR CRANIOFACIAL IMPLANTS WITH EMBEDDED TITANIUM MESH
- K021357 — MEDPOR PLUS ORBITAL VOLUME REPLACEMENT IMPANT
- K012350 — MEDPOR PLUS SURGICAL IMPLANT BIOMATERIAL
- K012108 — MEDPOR COATED TEAR DRAIN
- K010902 — MEDPOR QUAD MOTILITY IMPLANT
- K982040 — MEDPOR SURGICAL GRANULE IMPLANTS
- K981374 — POREX NOSTRIL RETAINERS
- K972034 — MEDPOR OCULAR CONFORMER
- K954939 — MEDPOR OCULAR SCREW & ACCESSORIES
- K952677 — MEDPOR BARRIER SURGICAL IMPLANT BIOMATERIAL
- K943275 — MEDPOR SURGICAL IMPLANT MATERIAL
Data sourced from openFDA. This site is unofficial and independent of the FDA.