510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K760726Substantially Equivalent

Electro-Keratotome, Line-Operated

Storz Instrument Co., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K760726 is the FDA 510(k) clearance record for ELECTRO-KERATOTOME, LINE-OPERATED, a class I device, cleared for Storz Instrument Co. on under FDA product code HNO (Keratome, Ac-Powered). FDA records list 101 510(k) clearances for Storz Instrument Co., from to . As of , FDA records show no recalls naming K760726.

Clearance record

Decision date
Received
(8 days to decision)
Product code
HNO Keratome, Ac-Powered
Regulation
21 CFR 886.4370
Device class
Class I
Review panel
Ophthalmic
Applicant
Storz Instrument Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code HNO

Trailing 12 months

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

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