Vitek, Inc.
Country not established
- Devices
- 1
What Vitek, Inc. makes
Vitek, Inc. manufactures the TRANSJAW™, a medical device designed for use in oral and maxillofacial procedures.
The TRANSJAW™ is classified as a Class I device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Transjaw(Tm) Ref K872815
510(k) 510(k)
Frequently asked questions
How many devices does Vitek, Inc. have in the registry?
The registry currently lists 1 device for Vitek, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vitek, Inc.'s devices?
Among its 1 most recently registered device, Vitek, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Vitek, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Vitek, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Vitek, Inc. in the registry?
The most recently registered devices listed for Vitek, Inc. include TRANSJAW(TM).