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FDA 510(k)

Vydence Family of Lasers

K-Number: K252753 · 2026-01-24

Decision Date2026-01-24
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Vydence Family of Lasers is a medical device manufactured by Vydence Medical Industria E Commercio Ltda. It received FDA 510(k) clearance on 2026-01-24 under approval number K252753. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vydence Family of Lasers?

Vydence Family of Lasers is a medical device that received FDA 510(k) clearance on 2026-01-24. It is manufactured by Vydence Medical Industria E Commercio Ltda. The 510(k) number is K252753.

When was Vydence Family of Lasers approved by the FDA?

Vydence Family of Lasers received FDA 510(k) clearance on 2026-01-24, under approval number K252753.

What company makes Vydence Family of Lasers?

Vydence Family of Lasers is manufactured by Vydence Medical Industria E Commercio Ltda.

What is the FDA product code for Vydence Family of Lasers?

The FDA product code for Vydence Family of Lasers is GEX. This falls under the Gastroenterology category.

Related Devices (Code: GEX)

Official Source

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