Odontit Systeme
Country not established
- Devices
- 1
What Odontit Systeme makes
Odontit Systeme manufactures the Odontit Osseointegrated Implant System, designed for dental applications to support fixed or removable prosthetics in patients with missing teeth.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The implants are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Odontit Osseointegrated Implants System Ref K915375
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Odontit Systeme have in the registry?
The registry currently lists 1 device for Odontit Systeme. Devices recorded under merged duplicate company entries are counted once.
Which registries list Odontit Systeme's devices?
Among its 1 most recently registered device, Odontit Systeme has devices listed in FDA 510(k) (1 device).
What risk classes do Odontit Systeme's devices fall under?
Among its 1 most recently registered device, the classes recorded for Odontit Systeme's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Odontit Systeme in the registry?
The most recently registered devices listed for Odontit Systeme include ODONTIT OSSEOINTEGRATED IMPLANTS SYSTEM.