Topia Medtech Limited
United KingdomFDA applicant, unverified FDA FEI 3043494619
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Topia Medtech Limited makes
Topia MedTech Limited manufactures the Alzevita, a medical device designed for the treatment of venous insufficiency or varicose veins, likely involving endovenous ablation or sclerotherapy techniques.
The company’s portfolio is regulated under FDA’s Class II device classification, with the Alzevita authorised via a 510(k) pathway. The device is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Alzevita Ref K252670
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3043494619
- Address
- 2 Falcon Gate,, Welwyn Garden City Herefordshire
Frequently asked questions
How many devices does TOPIA MEDTECH LIMITED have in the registry?
The registry currently lists 1 device for TOPIA MEDTECH LIMITED. Devices recorded under merged duplicate company entries are counted once.
Which registries list TOPIA MEDTECH LIMITED's devices?
Among its 1 most recently registered device, TOPIA MEDTECH LIMITED has devices listed in FDA 510(k) (1 device).
What risk classes do TOPIA MEDTECH LIMITED's devices fall under?
Among its 1 most recently registered device, the classes recorded for TOPIA MEDTECH LIMITED's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from TOPIA MEDTECH LIMITED in the registry?
The most recently registered devices listed for TOPIA MEDTECH LIMITED include Alzevita.