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
K221264Substantially Equivalent

FROG Forceps Valve (VAL1-F1-100)

FUJIFILM medwork GmbH, Hochstadt, DE / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K221264 is the FDA 510(k) clearance record for FROG Forceps Valve (VAL1-F1-100), a class II device, cleared for Fujifilm Medwork GmbH on under FDA product code ODC (Endoscope Channel Accessory). FDA's definition for product code ODC reads: "To give the endoscope channel additional or improved functionality". FDA records list 2 510(k) clearances for Fujifilm Medwork GmbH, from to . As of , FDA records show no recalls naming K221264.

Clearance record

Decision date
Received
(30 days to decision)
Product code
ODC Endoscope Channel Accessory
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Fujifilm Medwork GmbH Medworkring 1, Hochstadt, DE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code ODC

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