Mectron SpA
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Mectron SpA is a medical device manufacturer, with 321 devices listed in FDA GUDID (FDA Class II and I) as of 12 Nov 2026.
- Devices
- 321
Registry facts
- Registries
- FDA GUDID 321
- Device classes
- FDA Class II 276
- FDA Class I 45
- Identifiers
- DUNS 436664734
What Mectron SpA makes
The company produces dental ultrasonic surgical systems and associated handpiece tips, including periodontal, endodontic, and hard-tissue variants. These devices are designed for surgical precision, scaling, debridement, and torque adjustment in dental procedures. Reusable torque wrenches for ultrasonic systems are also part of the portfolio.
The portfolio includes devices classified as Class I and Class II under FDA regulations, with all products listed in the FDA’s Unique Device Identifier (UDI) database.
Catalogue
Search and filter all 321 devicesShowing 1-50 of 321
Company details
- DUNS number
- 436664734
- info@piezosurgery.us
- Phone
- +1 6144594922
Frequently asked questions
How many devices does MECTRON SPA have in the registry?
The registry currently lists 321 devices for MECTRON SPA. Devices recorded under merged duplicate company entries are counted once.
Which registries list MECTRON SPA's devices?
Among its 50 most recently registered devices, MECTRON SPA has devices listed in FDA GUDID (50 devices).
What risk classes do MECTRON SPA's devices fall under?
Among its 50 most recently registered devices, the classes recorded for MECTRON SPA's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from MECTRON SPA in the registry?
The most recently registered devices listed for MECTRON SPA include MECTRON OP1125, MECTRON OP1225, MECTRON EX0410 and MECTRON EX0510.