Lightsense Technologies, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Lightsense Technologies, Ltd. makes
Lightsense Technologies, Ltd. manufactures the S2 Pigment Removal System, a device designed for laser-based treatment of pigmented skin lesions, including tattoos and vascular lesions.
The S2 Pigment Removal System is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
S2 Pigment Removal System Ref K202848
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lightsense Technologies, Ltd. have in the registry?
The registry currently lists 1 device for Lightsense Technologies, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lightsense Technologies, Ltd.'s devices?
Among its 1 most recently registered device, Lightsense Technologies, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Lightsense Technologies, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lightsense Technologies, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lightsense Technologies, Ltd. in the registry?
The most recently registered devices listed for Lightsense Technologies, Ltd. include S2 Pigment Removal System.