Edge Medical Devices, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Edge Medical Devices, Ltd. makes
Edge Medical Devices, Ltd. manufactures the QUIX Digital Radiographic Upgrade, a device designed to enhance existing radiographic systems with digital imaging capabilities.
The QUIX Digital Radiographic Upgrade is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Quix Digital Radiographic Upgrade Ref K052661
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Edge Medical Devices, Ltd. have in the registry?
The registry currently lists 1 device for Edge Medical Devices, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Edge Medical Devices, Ltd.'s devices?
Among its 1 most recently registered device, Edge Medical Devices, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Edge Medical Devices, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Edge Medical Devices, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Edge Medical Devices, Ltd. in the registry?
The most recently registered devices listed for Edge Medical Devices, Ltd. include QUIX DIGITAL RADIOGRAPHIC UPGRADE.