Wartner Medical Products
CanadaFDA applicant, unverified
- Devices
- 3
What Wartner Medical Products makes
Wartner Medical Products manufactures wart removal systems, including the Wartner Wart Removal System, the Wartner Pro, and modifications to the Wartner Wart Removal System.
The company is based in the US, and its portfolio consists of Class II medical devices that are listed in the FDA 510(k) registry.
Catalogue
Modification To Wartner Wart Removal System Ref K011708
Regimes: 510(k) Registry: 510(k)Wartner Wart Removal System Ref K002714
Regimes: 510(k) Registry: 510(k)Wartner Pro Ref K030838
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wartner Medical Products have in the registry?
The registry currently lists 3 devices for Wartner Medical Products. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wartner Medical Products's devices?
Among its 3 most recently registered devices, Wartner Medical Products has devices listed in FDA 510(k) (3 devices).
What risk classes do Wartner Medical Products's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Wartner Medical Products's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wartner Medical Products in the registry?
The most recently registered devices listed for Wartner Medical Products include MODIFICATION TO WARTNER WART REMOVAL SYSTEM, WARTNER WART REMOVAL SYSTEM and WARTNER PRO.