510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K901275Substantially Equivalent

Retinal Taak

Alcon Surgical, Inc., Irvine CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K901275 is the FDA 510(k) clearance record for RETINAL TAAK, a class II device, cleared for Alcon Surgical, Inc. on under FDA product code HQW (Clip, Tantalum, Ophthalmic). FDA records list 3 510(k) clearances for Alcon Surgical, Inc., from to . As of , FDA records show no recalls naming K901275.

Clearance record

Decision date
Received
(4 days to decision)
Product code
HQW Clip, Tantalum, Ophthalmic
Regulation
21 CFR 886.3100
Device class
Class II
Review panel
Ophthalmic
Applicant
Alcon Surgical, Inc. 17701 Cowan Ave., Irvine CA
Third party review
No

Clearances, product code HQW

Trailing 12 months

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

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