MethodSense, Inc.
Country not established
- Devices
- 1
What MethodSense, Inc. makes
MethodSense, Inc. manufactures the NDOHD High Definition Imaging System, a device designed for high-resolution imaging applications in medical diagnostics.
The NDOHD High Definition Imaging System is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Ndohd High Definition Imaging System (Ndohd) Ref K131873
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does MethodSense, Inc. have in the registry?
The registry currently lists 1 device for MethodSense, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list MethodSense, Inc.'s devices?
Among its 1 most recently registered device, MethodSense, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do MethodSense, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for MethodSense, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from MethodSense, Inc. in the registry?
The most recently registered devices listed for MethodSense, Inc. include NDOHD HIGH DEFINITION IMAGING SYSTEM (NDOHD).