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
K926540Substantially Equivalent

Sopher and Bierer Ovum Forceps

Thomasville Medical Assoc., Alpharetta GA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K926540 is the FDA 510(k) clearance record for SOPHER AND BIERER OVUM FORCEPS, a class II device, cleared for Thomasville Medical Assoc. on under FDA product code HLZ (Electrode, Corneal). FDA records list 33 510(k) clearances for Thomasville Medical Assoc., from to . As of , FDA records show no recalls naming K926540.

Clearance record

Decision date
Received
(422 days to decision)
Product code
HLZ Electrode, Corneal
Regulation
21 CFR 886.1220
Device class
Class II
Review panel
Ophthalmic
Applicant
Thomasville Medical Assoc. 935 Cobblestone Ct., Alpharetta GA
510(k) summary
Statement
Third party review
No

Clearances, product code HLZ

Trailing 12 months
1 clearance under product code HLZ in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HLZ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260