United States Medical Corp.
Country not established
- Devices
- 1
What United States Medical Corp. makes
United States Medical Corp. manufactures a modified articulating endoscopic clamp, which is a specialized medical device used in endoscopic procedures.
This device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Modified Articulating Endoscopic Clamp Ref K925150
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does United States Medical Corp. have in the registry?
The registry currently lists 1 device for United States Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list United States Medical Corp.'s devices?
Among its 1 most recently registered device, United States Medical Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do United States Medical Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for United States Medical Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from United States Medical Corp. in the registry?
The most recently registered devices listed for United States Medical Corp. include MODIFIED ARTICULATING ENDOSCOPIC CLAMP.