Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K041096Substantially Equivalent

Wagner Steriset Sterilization Container

Wagner GmbH, Bristol WI / Traditional, Substantially Equivalent

K041096 is the FDA 510(k) clearance record for WAGNER STERISET STERILIZATION CONTAINER, a class II device, cleared for Wagner GmbH on under FDA product code FRG (Wrap, Sterilization). FDA records list one 510(k) clearance for Wagner GmbH. As of , FDA records show no recalls naming K041096.

Clearance record

Decision date
Received
(402 days to decision)
Product code
FRG Wrap, Sterilization
Regulation
21 CFR 880.6850
Device class
Class II
Review panel
General Hospital
Applicant
Wagner GmbH 22411 60th St., Bristol WI
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FRG

Trailing 12 months
5 clearances under product code FRG in the twelve months to October 2026, May 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code FRG, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20260
March 20260
April 20260
May 20262
June 20260
July 20261
August 20260
September 20260
October 20260