Bioticsai, Inc.
United Statesfrom the FDA registration address FDA FEI 3047889344
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Bioticsai, Inc. makes
Bioticsai, Inc. develops AI-driven medical imaging software for diagnostic support, focusing on automated analysis of radiographic and ultrasound images to assist radiologists in identifying abnormalities.
The company’s portfolio is regulated under FDA’s Class II device classification, with products authorised via the 510(k) pathway. Bioticsai, Inc. is headquartered in the United States.
Catalogue
BioticsAI Ref K250959
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3047889344
- Address
- 455 Market St Ste 1940 Pmb 696426, San Francisco, CA, 94105
Frequently asked questions
How many devices does Bioticsai, Inc. have in the registry?
The registry currently lists 1 device for Bioticsai, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bioticsai, Inc.'s devices?
Among its 1 most recently registered device, Bioticsai, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Bioticsai, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bioticsai, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bioticsai, Inc. in the registry?
The most recently registered devices listed for Bioticsai, Inc. include BioticsAI.