Dr. Yglo Skin Tag Remover
K-Number: K251524 · 2026-01-12
ApplicantTheotclab Healthcare B.V.
Decision Date2026-01-12
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Dr. Yglo Skin Tag Remover is a medical device manufactured by Theotclab Healthcare B.V.. It received FDA 510(k) clearance on 2026-01-12 under approval number K251524. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Dr. Yglo Skin Tag Remover?
Dr. Yglo Skin Tag Remover is a medical device that received FDA 510(k) clearance on 2026-01-12. It is manufactured by Theotclab Healthcare B.V.. The 510(k) number is K251524.
When was Dr. Yglo Skin Tag Remover approved by the FDA?
Dr. Yglo Skin Tag Remover received FDA 510(k) clearance on 2026-01-12, under approval number K251524.
What company makes Dr. Yglo Skin Tag Remover?
Dr. Yglo Skin Tag Remover is manufactured by Theotclab Healthcare B.V..
What is the FDA product code for Dr. Yglo Skin Tag Remover?
The FDA product code for Dr. Yglo Skin Tag Remover is GEH.
Other Devices by Theotclab Healthcare B.V.
Related Devices (Code: GEH)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.