Advanced Cryo Skin Tag Remover (Advanced Skin Tag Remover)

FDA 510(k) K252198 · Medical Brands Laboratories B.V.

Substantially Equivalent

510(k) numberK252198

Submission

Device name
Advanced Cryo Skin Tag Remover (Advanced Skin Tag Remover)
Applicant
Medical Brands Laboratories B.V.
Diemen, NL
Received
July 14, 2025
Decision date
April 2, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GEH – Unit, Cryosurgical, Accessories
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4350
Specialty
General, Plastic Surgery

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More from Cryosurgery, Inc.

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Questions and answers

When was Advanced Cryo Skin Tag Remover (Advanced Skin Tag Remover) cleared by the FDA?

Advanced Cryo Skin Tag Remover (Advanced Skin Tag Remover) (K252198) received a 510(k) decision of Substantially Equivalent on April 2, 2026, 262 days after the submission was received.

What is the product code of K252198?

The FDA product code is GEH – Unit, Cryosurgical, Accessories, a Class II (moderate risk) device regulated under 21 CFR 878.4350.