510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K950599Substantially Equivalent

Stors Scleral Sponge II (Lincoff Design)

Storz Ophthalmics, Inc., Clearwater FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K950599 is the FDA 510(k) clearance record for STORS SCLERAL SPONGE II (LINCOFF DESIGN), a class II device, cleared for Storz Ophthalmics, Inc. on under FDA product code HQX (Implant, Orbital, Extra-Ocular). FDA records list 2 510(k) clearances for Storz Ophthalmics, Inc., from to . As of , FDA records show no recalls naming K950599.

Clearance record

Decision date
Received
(21 days to decision)
Product code
HQX Implant, Orbital, Extra-Ocular
Regulation
21 CFR 886.3340
Device class
Class II
Review panel
Ophthalmic
Applicant
Storz Ophthalmics, Inc. 21 Park Pl. Blvd. N., Clearwater FL
510(k) summary
Summary
Third party review
No

Clearances, product code HQX

Trailing 12 months

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

FDA records show no clearances under product code HQX in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HQX, 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