FDA 510(k) Applications Submitted by OCULO PLASTIK, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K040689 03/16/2004 EYE SPHERE IMPLANTS OCULO PLASTIK, INC.
K073293 11/23/2007 DURETTE IMPLANT OCULO PLASTIK, INC.
K112176 07/28/2011 SILICONE SPHERES OCULO PLASTIK, INC.


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