Scano, Inc.
Country not established
- Devices
- 1
What Scano, Inc. makes
Scano, Inc. manufactures ultrasound systems designed for measuring soft tissue depth, specifically the SCANO 731B and 731C models. These devices are intended for clinical applications in dermatology and related specialties to assess skin and subcutaneous tissue layers.
The company’s portfolio is regulated under FDA Class II devices, with relevant products listed via the 510(k) clearance pathway. These devices are intended for use within the United States, adhering to applicable medical device regulations.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Scano, Inc. have in the registry?
The registry currently lists 1 device for Scano, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Scano, Inc.'s devices?
Among its 1 most recently registered device, Scano, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Scano, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Scano, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Scano, Inc. in the registry?
The most recently registered devices listed for Scano, Inc. include SCANO 731B & 731C ULTRASOUND SOFT TIS DEPT MEAS SY.