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Parker Quality & Compliance

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510(k) clearance

Dynamis Pro Family

FDA 510(k) source

510(k) number
K252723
Applicant
Fotona D.O.O.
Decision date
Sep 19, 2026
Date received
Aug 28, 2025
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
Ljubljana, SI