Mastel Precision, Inc.
Country not established
- Devices
- 1
What Mastel Precision, Inc. makes
Mastel Precision, Inc. manufactures the MASTEL 1 FOLDER IMPLANTATION SYSTEM, a Class I medical device.
The company is based in the US and its device is listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Mastel 1 Folder Implantation System Ref K022723
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mastel Precision, Inc. have in the registry?
The registry currently lists 1 device for Mastel Precision, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mastel Precision, Inc.'s devices?
Among its 1 most recently registered device, Mastel Precision, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Mastel Precision, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mastel Precision, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Mastel Precision, Inc. in the registry?
The most recently registered devices listed for Mastel Precision, Inc. include MASTEL 1 FOLDER IMPLANTATION SYSTEM.