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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