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FDA 510(k)

Dr. Yglo Skin Tag Remover

K-Number: K251524 · 2026-01-12

Decision Date2026-01-12
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Dr. Yglo Skin Tag Remover is the device name listed in this FDA 510(k) record. The listed applicant is Theotclab Healthcare B.V.. It received FDA 510(k) clearance on 2026-01-12 under 510(k) 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. The listed applicant is Theotclab Healthcare B.V.. The 510(k) number is K251524.

When did Dr. Yglo Skin Tag Remover receive FDA 510(k) clearance?

Dr. Yglo Skin Tag Remover received FDA 510(k) clearance on 2026-01-12, under 510(k) number K251524.

Who is the listed applicant for Dr. Yglo Skin Tag Remover?

The FDA 510(k) record lists Theotclab Healthcare B.V. as the applicant. This does not by itself establish the device manufacturer.

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 records listing Theotclab Healthcare B.V. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: GEH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.