Medical Device Manufacturer · IT , Carasco

Mectron S.P.A. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 2009

Recent clearances: turbodent touch, MT-Bone, Combi Touch

Total

Cleared

Denied

Mectron S.P.A. has 13 FDA 510(k) cleared dental devices. Based in Carasco, IT.

Latest FDA clearance: May 2025. Active since 2009.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Regulatory Technology Services, LLC, Backroads Consulting, Inc. and Donawa Lifescience Consulting Srl.

Mectron S.P.A. is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Mectron S.P.A.

13 devices

1-12 of 13

PIEZOSURGERY TOUCH, PIEZOSURGERY WHITE

MULTIPIEZO PRO, MULTIPIEZO

COMPACT PIEZO P2K, POWERCARE

K102218 · ELC

Dental · 171d

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: Apr 30, 2026

Mectron S.P.A. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Mectron S.P.A.

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