Xf Agencija Limited
ChinaFDA applicant, unverified FDA FEI 3026322014
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Nooro Body & Foot Stimulator (SM9141, SM9142) Ref K243334
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3026322014
- Address
- Room 1502,Beverly House,93-107 Lockhart Road, Wanchai Hong Kong
Frequently asked questions
How many devices does Xf Agencija Limited have in the registry?
The registry currently lists 1 device for Xf Agencija Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Xf Agencija Limited's devices?
Among its 1 most recently registered device, Xf Agencija Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Xf Agencija Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Xf Agencija Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Xf Agencija Limited in the registry?
The most recently registered devices listed for Xf Agencija Limited include Nooro Body & Foot Stimulator (SM9141, SM9142).