510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K935302Substantially Equivalent

Osher Surgical Gonio/posterior Pole Lens

Ocular Instruments, Inc., Bellevue WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K935302 is the FDA 510(k) clearance record for OSHER SURGICAL GONIO/POSTERIOR POLE LENS, a class I device, cleared for Ocular Instruments, Inc. on under FDA product code HKS (Prism, Gonioscopic). FDA records list 50 510(k) clearances for Ocular Instruments, Inc., from to . As of , FDA records show no recalls naming K935302.

Clearance record

Decision date
Received
(150 days to decision)
Product code
HKS Prism, Gonioscopic
Regulation
21 CFR 886.1660
Device class
Class I
Review panel
Ophthalmic
Applicant
Ocular Instruments, Inc. 2255 116th Ave., NE, Bellevue WA
510(k) summary
Statement
Third party review
No

Clearances, product code HKS

Trailing 12 months

FDA records hold no clearances under product code HKS in the trailing twelve months.

FDA records show no clearances under product code HKS in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HKS, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260