FDA 510(k) clearance · back to tracker

Nd:YAG & Alexandrite Long Pulse Laser Therapy Instrument (LPDuo)

Keyue (Hangzhou) Medical Information Technology Co., Ltd. cleared K261572 on 2026-10-13, decision: substantially equivalent

K-number

K261572

Sponsor

Keyue (Hangzhou) Medical Information Technology Co., Ltd.

Device

Nd:YAG & Alexandrite Long Pulse Laser Therapy Instrument (LPDuo)

Class

Class II

Decision

Substantially Equivalent

Decision date

2026-10-13

Product code

GEX

Advisory committee

General, Plastic Surgery

Medical specialty

General, Plastic Surgery

Regulation number

878.4810

Official FDA record

Open K261572on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

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Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.