S4S UK, Ltd.
United KingdomFDA 510(k) applicant, unverified
- Devices
- 1
What S4S UK, Ltd. makes
S4S UK, Ltd. manufactures the Morpheus device, a non-invasive skin remodeling system designed for aesthetic treatments such as wrinkle reduction and skin tightening.
The Morpheus device is classified as Class II under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Morpheus Ref K210636
510(k) 510(k)
Frequently asked questions
How many devices does S4S UK, Ltd. have in the registry?
The registry currently lists 1 device for S4S UK, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list S4S UK, Ltd.'s devices?
Among its 1 most recently registered device, S4S UK, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do S4S UK, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for S4S UK, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from S4S UK, Ltd. in the registry?
The most recently registered devices listed for S4S UK, Ltd. include Morpheus.