Crantec Co.
Country not established
- Devices
- 1
What Crantec Co. makes
Crantec Co. manufactures the PRESTITCH, which is a medical device. This product is categorized as a surgical instrument.
The device is classified as Class I and is listed within the FDA 510(k) regulatory database. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Prestitch Ref K910449
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Crantec Co. have in the registry?
The registry currently lists 1 device for Crantec Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Crantec Co.'s devices?
Among its 1 most recently registered device, Crantec Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Crantec Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Crantec Co.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Crantec Co. in the registry?
The most recently registered devices listed for Crantec Co. include PRESTITCH.