Ultraspect, Ltd.
IsraelFDA applicant, unverified
- Devices
- 6
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Wbr Xpress Pet Ref K103710
Regimes: 510(k) Registry: 510(k)Xact.cardiac & Xpress.cardiac Ref K050815
Regimes: 510(k) Registry: 510(k)Wbr XPRESS3.CARDIAC Ref K081201
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Wbr-Fhr, Wbr-Fwb Ref K040370
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ultraspect, Ltd. have in the registry?
The registry currently lists 6 devices for Ultraspect, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ultraspect, Ltd.'s devices?
Among its 6 most recently registered devices, Ultraspect, Ltd. has devices listed in FDA 510(k) (6 devices).
What risk classes do Ultraspect, Ltd.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Ultraspect, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ultraspect, Ltd. in the registry?
The most recently registered devices listed for Ultraspect, Ltd. include WBR XPRESS PET, XACT.CARDIAC & XPRESS.CARDIAC, WBR XPRESS3.CARDIAC and WBR XPRESS.CARDIAC, WBR XPRESS.BONE; WBR XACT.CARDIAC, WBR XACT.BONE.