Medicis Technologies Corporation
United StatesFDA applicant, unverified
- Devices
- 2
What Medicis Technologies Corporation makes
Medicis Technologies Corporation manufactures ultrasound-guided lipolysis systems, including the LIPSONIX® SYSTEM MODEL 2 and the LIPSONIX SYSTEM (Model 1 P00XXXX), designed for non-surgical fat reduction procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Lipsonix(R) System Model 2 Ref K112626
Regimes: 510(k) Registry: 510(k)Liposonix System, Model 1 P00XXXX Ref K100874
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medicis Technologies Corporation have in the registry?
The registry currently lists 2 devices for Medicis Technologies Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medicis Technologies Corporation's devices?
Among its 2 most recently registered devices, Medicis Technologies Corporation has devices listed in FDA 510(k) (2 devices).
What risk classes do Medicis Technologies Corporation's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Medicis Technologies Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medicis Technologies Corporation in the registry?
The most recently registered devices listed for Medicis Technologies Corporation include LIPSONIX(R) SYSTEM MODEL 2 and LIPOSONIX SYSTEM, MODEL 1 P00XXXX.