Odontit S.A.
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Odontit S.A. is a medical device manufacturer, with 329 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 13 Nov 2026.
- Devices
- 329
Registry facts
- Registries
- FDA GUDID 326
- FDA 510(k) 3
- Device classes
- FDA Class II 329
- Identifiers
- DUNS 972044937
What Odontit S.A. makes
Odontit S.A. manufactures two-piece screw endosteal dental implants designed for osseointegration in the jawbone, as well as dental bone matrix implants derived from animal sources to support bone regeneration and grafting procedures.
Their products are classified as Class II medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database.
Catalogue
Search and filter all 329 devicesShowing 1-50 of 329
Company details
- DUNS number
- 972044937
- info@odontit.com
- Phone
- +541148250221
Frequently asked questions
How many devices does ODONTIT S.A. have in the registry?
The registry currently lists 329 devices for ODONTIT S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list ODONTIT S.A.'s devices?
Among its 50 most recently registered devices, ODONTIT S.A. has devices listed in FDA GUDID (50 devices).
What risk classes do ODONTIT S.A.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for ODONTIT S.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ODONTIT S.A. in the registry?
The most recently registered devices listed for ODONTIT S.A. include Odontit EB2213, SCIOGRAFT SG-250-S, Odontit RA43-UCLA-CR and Odontit RA43-HIA.