Sanker Intl., Inc.
Country not established
- Devices
- 1
What Sanker Intl., Inc. makes
Sanker Intl., Inc. manufactures the HYDROT, a device designed for hydrotherapy applications, likely used in physical therapy or wound care to deliver controlled water-based treatments.
The HYDROT is classified as a Class II medical device in the U.S. and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Hydrot Ref K930918
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sanker Intl., Inc. have in the registry?
The registry currently lists 1 device for Sanker Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sanker Intl., Inc.'s devices?
Among its 1 most recently registered device, Sanker Intl., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sanker Intl., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sanker Intl., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sanker Intl., Inc. in the registry?
The most recently registered devices listed for Sanker Intl., Inc. include HYDROT.