Sofradim Production
Sofradim Production holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2026, with 1 FDA device recall on record.
Top product codes for Sofradim Production
FDA recalls by Sofradim Production
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Sofradim Production
- K253956 — ProGrip advanced self-gripping polypropylene mesh (ADG1510, ADG2015, ADG3020, ADG4030)
- K250869 — Parietene Macroporous Mesh (PPM5050 )
- K243315 — ProGrip Self-Gripping Polypropylene Mesh
- K233661 — Transorb Self-Gripping Resorbable Mesh
- K232373 — Progrip Self-Gripping Polypropylene Mesh
- K223218 — Parietene Macroporous Mesh
- K220586 — Symbotex Composite Mesh, ProGrip Self-Gripping Polyester Mesh, Parietex Hydrophilic 2D 3D Anatomical Mesh, Versatex Monofilament Mesh
- K192443 — Dextile Anatomical Mesh
- K173796 — Parietex Surgical Mesh (modified into Parietex Hydrophilic 2D, 3D, Anatomical Mesh), Parietex Composite Mesh (PCO and PCO-OS references), Parietex Optimized Composite Mesh (PCO-X, PCO-FX and PCO-OSX references)
- K172395 — Duatene bilayer mesh
- K163212 — Parietene DS Composite Mesh
- K150091 — Versatex Monofilament Mesh
- K143386 — Progrip Laparoscopic Self-Fixating Mesh
- K142908 — Parietex Monofilament Polyester Mesh (new name: Parietex Lightweight Mesh), Parietex Composite Mono PM Mesh (new name: Parietex Composite Parastomal Mesh), Parietex Composite Ventral Patch, Symbotex Composite Mesh
- K142900 — Parietex Progrip Mesh (new name: Progrip Self-Gripping Polyester Mesh), Parietex Plug and Patch (new name : Parietex Plug and Patch System), Progrip Laparoscopic Self-Fixating Mesh
- K142091 — PARIETENE MACROPOROUS MESH
- K140941 — PROGRIP SELF-GRIPPING POLYPROPYLENE MESH, PARIETENE FLAT SHEET MESH
- K131969 — SYMBOTEX(TM) COMPOSITE MESH
- K123479 — PROGRIP LAPAROSCOPIC SELF-FIXATING MESH
- K120897 — PROGRIP LAPARSCOPIC SELF-FIXATING MESH
- K120506 — PARIETEX COMPOSITE VENTRAL PATCH
- K110663 — PAIRETEX OPTIMIZED COMPOSITE MESH (PCO-FX REFRENCES)
- K110815 — PARIETEX OPTIMIZED COMPOSTIE MESH
- K110816 — PARIETEX OPTIMIZED COMPOSITE MESH (PCO-OSX REFERENCES)
- K103682 — PARIETEX PROGRIP
- K101519 — PARIETEX PLUG AND PATCH
- K101197 — PARIE TENE PROGRIP MESH
- K090858 — PARIETEX MONOFILAMENT POLYESTER MESH
- K081126 — PARIETEX COMPOSITE MONO PM MESH
- K081050 — PARIETEX PROGRIP MESH
- K073287 — PREVADH MESH
- K072951 — PARIETENE DUO AND QUADRA POLYPROPYLENE MESHES
- K071629 — PARIETEX POLYESTER MESH WITH INTRODUCER
- K051503 — UGYTEX SUAL KNIT MESH
- K050187 — PARIETEX COMPOSITE PCO-OS AND PCO-OB MESHES
- K041176 — URETEX TO TRANS-OBTURATOR URETHRAL SUPPORT SYSTEM
- K040998 — MODIFICATION TO PARIETEX COMPOSITE (PCO) MESH
- K033376 — UGYTEX MESH
- K032093 — PARIEFIX
- K012949 — URETEX SUP PUBOURETHRAL SLING
- K003990 — SOFRADIM PARIETEX SURGICAL MESHES
- K991400 — PARIETENE POLYPROPYLENE MESH
Data sourced from openFDA. This site is unofficial and independent of the FDA.