Cartessa Aesthetics
Country not established FDA establishment FEI 3013602304
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
What Cartessa Aesthetics makes
Cartessa Aesthetics manufactures the SubNovii Advanced Plasma Technology, which is a Class II medical device used for aesthetic treatments.
The company is based in the US, and its device is listed in the FDA 510(k) registry, indicating it has been cleared for marketing in the United States.
Catalogue
SubNovii Advanced Plasma Technology Ref K201738
510(k) 510(k)
Company details
- FDA FEI number
- 3013602304
- Address
- 175 Broadhollow Rd Ste 220, Melville, NY, 11747
Frequently asked questions
How many devices does CARTESSA AESTHETICS have in the registry?
The registry currently lists 1 device for CARTESSA AESTHETICS. Devices recorded under merged duplicate company entries are counted once.
Which registries list CARTESSA AESTHETICS's devices?
Among its 1 most recently registered device, CARTESSA AESTHETICS has devices listed in FDA 510(k) (1 device).
What risk classes do CARTESSA AESTHETICS's devices fall under?
Among its 1 most recently registered device, the classes recorded for CARTESSA AESTHETICS's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from CARTESSA AESTHETICS in the registry?
The most recently registered devices listed for CARTESSA AESTHETICS include SubNovii Advanced Plasma Technology.