Provino
DenmarkFDA applicant, unverified
- Devices
- 1
What Provino makes
Provino manufactures the SOPHYCAMERA DSM 315, a medical imaging device designed for dermatological examinations, enabling high-resolution capture of skin conditions.
The SOPHYCAMERA DSM 315 is classified as a Class I device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Sophycamera Dsm 315 Ref K903030
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Provino have in the registry?
The registry currently lists 1 device for Provino. Devices recorded under merged duplicate company entries are counted once.
Which registries list Provino's devices?
Among its 1 most recently registered device, Provino has devices listed in FDA 510(k) (1 device).
What risk classes do Provino's devices fall under?
Among its 1 most recently registered device, the classes recorded for Provino's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Provino in the registry?
The most recently registered devices listed for Provino include SOPHYCAMERA DSM 315.