Oculo Plastik, Inc.
Oculo Plastik, Inc. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 2013.
Name variants for Oculo Plastik, Inc.
as filed with FDA- Oculo Plastik, Inc.
- Oculo-Plastik, Inc.
Top product codes for Oculo Plastik, Inc.
Recent clearances by Oculo Plastik, Inc.
- K123764 — DURETTE OCULAR IMPLANT
- K112176 — SILICONE SPHERES
- K073293 — DURETTE IMPLANT
- K040689 — EYE SPHERE IMPLANTS
- K934834 — EPTFE SHEET COVERING FOR OCULAR IMPLANT
- K915630 — OPHTIMPLANT
- K901002 — O'DONNELL, SOCKET RECONSTRUCTION PROSTHESES
- K900929 — PUTTERMAN-SCOTT, SOCKET RECONSTRUCTION BILATERAL
- K900927 — CODERE-DURETTE ORBITAL FLOOR IMPLANT
- K900928 — COX MALAR EMINENCE IMPLANTS
- K900930 — SPIVEY-ALLEN ORBITAL FLOOR IMPLANT
- K900080 — NEW IOWA MOTILITY IMPLANT
- K900081 — NEW ALLEN IMPLANT
Data sourced from openFDA. This site is unofficial and independent of the FDA.