Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K242288Substantially Equivalent

Advanced Cryo Wart Remover

Medical Brands Laboratories B.V., Diemen, NL / Traditional, Substantially Equivalent

K242288 is the FDA 510(k) clearance record for Advanced Cryo Wart Remover, a class II device, cleared for Medical Brands Laboratories B.V. on under FDA product code GEH (Unit, Cryosurgical, Accessories). FDA records list 2 510(k) clearances for Medical Brands Laboratories B.V., from to . As of , FDA records show no recalls naming K242288.

Clearance record

Decision date
Received
(172 days to decision)
Product code
GEH Unit, Cryosurgical, Accessories
Regulation
21 CFR 878.4350
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Medical Brands Laboratories B.V. Weesperstraat 114, Diemen, NL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GEH

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