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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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