Sopro - Acteon Group
Country not established
- Devices
- 4
What Sopro - Acteon Group makes
Sopro manufactures intraoral dental scanners, including the PSPIX 2 system with interchangeable imaging plates (sizes 0–3) for digital dental impressions, and the SOPIX and SOPIX INSIDE series for intraoral and indirect scanning. The company also produces the S698 Symbioz flow, a dental unit designed for water and air flow control in clinical procedures.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records in the U.S. registry. The manufacturer is based in the United States.
Catalogue
- Regimes: CE MDR 510(k) Registry: 510(k)
Sopix Ref K142995
Regimes: 510(k) Registry: 510(k)Sopix Inside, SOPIX2 Inside Ref K140013
Regimes: CE MDR 510(k) Registry: 510(k)S698 Symbioz flow Ref K153367
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sopro - Acteon Group have in the registry?
The registry currently lists 4 devices for Sopro - Acteon Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sopro - Acteon Group's devices?
Among its 4 most recently registered devices, Sopro - Acteon Group has devices listed in FDA 510(k) (4 devices).
What risk classes do Sopro - Acteon Group's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Sopro - Acteon Group's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sopro - Acteon Group in the registry?
The most recently registered devices listed for Sopro - Acteon Group include PSPIX 2 scanner, Imaging Plate Size 0 for PSPIX2 scanner, Imaging Plate Size 1 for PSPIX2 scanner, Imaging Plate Size 2 for PSPIX2 scanner, Imaging Plate Size 3 for PSPIX2 scanner, SOPIX, SOPIX INSIDE, SOPIX2 INSIDE and S698 Symbioz flow.