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FDA 510(k) Applications Submitted by MECTRON S.P.A.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K231391
05/12/2023
Combi Touch
Mectron S.p.A.
K122322
08/01/2012
PIEZOSURGERY TOUCH
MECTRON S.P.A.
K102218
08/06/2010
COMPACT PIEZO P2K, POWERCARE
MECTRON S.P.A.
K132848
09/11/2013
PIEZOSURGERY FLEX
MECTRON S.P.A.
K092951
09/24/2009
STARLIGHT PRO AND SILIVERLIGHT DENTAL CURING LIGHTS
MECTRON S.P.A.
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