Waldmann Lighting Co.
Also registered as Waldmann Lighting
United Statesfrom the FDA registration address FDA FEI 1000279762
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Halux Iris Examination And Surgical Lamp Ref K053364
Regimes: 510(k) Registry: 510(k)Uv 8001K, Puva 800, Puva 180/200 1000 Ref K841795
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000279762
- Address
- 9 WEST CENTURY DRIVE, Wheeling, IL, 60090
Frequently asked questions
How many devices does Waldmann Lighting Co. have in the registry?
The registry currently lists 2 devices for Waldmann Lighting Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Waldmann Lighting Co.'s devices?
Among its 2 most recently registered devices, Waldmann Lighting Co. has devices listed in FDA 510(k) (2 devices).
What risk classes do Waldmann Lighting Co.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Waldmann Lighting Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Waldmann Lighting Co. in the registry?
The most recently registered devices listed for Waldmann Lighting Co. include HALUX IRIS EXAMINATION AND SURGICAL LAMP and UV 8001K, PUVA 800, PUVA 180/200 1000.