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510(k) K123764

DURETTE OCULAR IMPLANT by Oculo-Plastik, Inc. — Product Code HPZ

K123764 is an FDA 510(k) premarket notification submitted by Oculo-Plastik, Inc. for the device "DURETTE OCULAR IMPLANT". The FDA issued a decision of Substantially Equivalent on January 31, 2013. The device falls under product code HPZ (Implant, Eye Sphere), a Class II device regulated under 21 CFR 886.3320.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 31, 2013
Date Received
December 7, 2012
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Implant, Eye Sphere
Device Class
Class II
Regulation Number
886.3320
Review Panel
OP
Submission Type

Other clearances for product code HPZ

  • K212741 — EZYPOR (June 24, 2022)
  • K110554 — BIOCERAMIC ORBITAL IMPLANT, ORBTEX (November 2, 2011)
  • K112176 — SILICONE SPHERES (September 15, 2011)
  • K083342 — ORBITAL RECONSTRUCTIVE IMPLANT II (March 12, 2009)
  • K082850 — EYE SPHERES (February 27, 2009)
  • K073293 — DURETTE IMPLANT (March 19, 2008)
  • K071335 — MEDPOR ATTRACTOR IMPLANT (August 8, 2007)
  • K070130 — ORBITAL RECONSTRUCTIVE IMPLANT (April 19, 2007)
  • K053298 — ALPHASPHERE ORBITAL IMPLANT (May 9, 2006)
  • K040851 — MEDPOR ATTRACTOR MAGNETIC COUPLING SYSTEM (July 16, 2004)

FDA data resources