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
K022751Substantially Equivalent

Reprocessed Used Disposable Hot and Cold Biopsy Forceps

Medical Device Services, St. George UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K022751 is the FDA 510(k) clearance record for REPROCESSED USED DISPOSABLE HOT AND COLD BIOPSY FORCEPS, a class II device, cleared for Medical Device Services on under FDA product code KGE (Forceps, Biopsy, Electric). FDA records list 6 510(k) clearances for Medical Device Services, from to . As of , FDA records show no recalls naming K022751.

Clearance record

Decision date
Received
(77 days to decision)
Product code
KGE Forceps, Biopsy, Electric
Regulation
21 CFR 876.4300
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Medical Device Services 144 W. Brigham Rd., St. George UT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KGE

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