Porex Surgical, Inc.
FDA 510(k) medical device clearances.
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.