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/ G.N.S Neolaser , Ltd.
G.N.S Neolaser , Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K250113
neoLaser Laser Surgery Fibers
March 13, 2025
K152722
neoV980 & neoV1470 Diode Lasers
December 8, 2015
K133006
NEOV DIODE LASER FAMILY
April 17, 2014