Vitrotec, Inc.
Country not established
- Devices
- 1
What Vitrotec, Inc. makes
Vitrotec, Inc. manufactures the Vitrotec True Light Endoilluminator (100-S), which is a surgical device used for illumination during endoscopic procedures.
The company is based in the United States, and its product portfolio includes Class II medical devices that are listed in the FDA 510(k) regulatory registry.
Catalogue
Vitrotec True Light Endoilluminator (100-S) Ref K964555
510(k) 510(k)
Frequently asked questions
How many devices does Vitrotec, Inc. have in the registry?
The registry currently lists 1 device for Vitrotec, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vitrotec, Inc.'s devices?
Among its 1 most recently registered device, Vitrotec, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Vitrotec, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Vitrotec, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vitrotec, Inc. in the registry?
The most recently registered devices listed for Vitrotec, Inc. include VITROTEC TRUE LIGHT ENDOILLUMINATOR (100-S).