Ambicare Health, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Ambicare Health, Ltd. makes
Ambicare Health, Ltd. manufactures the Lustre PRO Light System, a medical device designed for photodynamic therapy applications in dermatology, utilizing specific light wavelengths to treat skin conditions.
The Lustre PRO Light System is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Lustre PRO Light System Ref K143713
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ambicare Health, Ltd. have in the registry?
The registry currently lists 1 device for Ambicare Health, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ambicare Health, Ltd.'s devices?
Among its 1 most recently registered device, Ambicare Health, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Ambicare Health, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ambicare Health, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ambicare Health, Ltd. in the registry?
The most recently registered devices listed for Ambicare Health, Ltd. include Lustre PRO Light System.