Newlands Clinical Trials, Ltd.
Country not established
- Devices
- 1
What Newlands Clinical Trials, Ltd. makes
Newlands Clinical Trials, Ltd. manufactures the VEINWAVE and TC3000, which are medical devices used for vascular treatments.
These Class II devices are listed in the FDA 510(k) registry, and the company is based in the US.
Catalogue
Veinwave, TC3000 Ref K083352
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Newlands Clinical Trials, Ltd. have in the registry?
The registry currently lists 1 device for Newlands Clinical Trials, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Newlands Clinical Trials, Ltd.'s devices?
Among its 1 most recently registered device, Newlands Clinical Trials, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Newlands Clinical Trials, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Newlands Clinical Trials, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Newlands Clinical Trials, Ltd. in the registry?
The most recently registered devices listed for Newlands Clinical Trials, Ltd. include VEINWAVE, TC3000.