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Parker Quality & Compliance

PQC Reg Watch

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510(k) clearance

B`orze Inc Laser Family (Sorren/Adonis)

FDA 510(k) source

510(k) number
K263063
Applicant
Borze, Inc.
Decision date
Oct 30, 2026
Date received
Sep 1, 2026
Decision
Substantially Equivalent
Clearance type
Traditional
Product code
GEX
Device type
Powered Laser Surgical Instrument
Device class
Class II
Regulation
21 CFR 878.4810
Advisory committee
General, Plastic Surgery
Statement or summary
Summary
Third party
N
Location
Boise, ID, US