General Project S.r.l.
Country not established
- Devices
- 5
What General Project S.r.l. makes
General Project S.R.L. manufactures aesthetic and dermatological devices, including the MED Sculpt for non-invasive body contouring, the MED Contour for skin tightening, and the MED Flash II and Axiom Intensive Pulsed Light Systems for skin rejuvenation and pigmentation treatment. The MC1 Plus is also part of their portfolio, likely for similar therapeutic applications.
All listed devices fall under Class II regulatory classification and are authorised via the FDA’s 510(k) pathway. The company is based in the United States and maintains registrations through the FDA’s 510(k) clearance system.
Catalogue
Med Sculpt Ref K053041
Regimes: 510(k) Registry: 510(k)Med Contour Ref K091615
Regimes: 510(k) Registry: 510(k)Med Flash Ii Intense Pulsed Light System. Ref K051508
Regimes: 510(k) Registry: 510(k)Axiom Pulsed Light System Ref K062312
Regimes: 510(k) Registry: 510(k)MC1 Plus Ref K161502
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does General Project S.R.L. have in the registry?
The registry currently lists 5 devices for General Project S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list General Project S.R.L.'s devices?
Among its 5 most recently registered devices, General Project S.R.L. has devices listed in FDA 510(k) (5 devices).
What risk classes do General Project S.R.L.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for General Project S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from General Project S.R.L. in the registry?
The most recently registered devices listed for General Project S.R.L. include MED SCULPT, MED CONTOUR, MED FLASH II INTENSE PULSED LIGHT SYSTEM. and AXIOM PULSED LIGHT SYSTEM.