Ismart Marketing Svcs, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Ismart Marketing Svcs, Ltd. makes
Ismart Marketing Svcs, Ltd. manufactures the faceLITE, a device designed for cosmetic skin rejuvenation using light-based technology.
The faceLITE is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
faceLITE Ref K191629
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ismart Marketing Svcs, Ltd. have in the registry?
The registry currently lists 1 device for Ismart Marketing Svcs, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ismart Marketing Svcs, Ltd.'s devices?
Among its 1 most recently registered device, Ismart Marketing Svcs, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Ismart Marketing Svcs, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ismart Marketing Svcs, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ismart Marketing Svcs, Ltd. in the registry?
The most recently registered devices listed for Ismart Marketing Svcs, Ltd. include faceLITE.