Affirm Medical Technologies II, LLC
United Statesfrom the FDA registration address FDA FEI 3047890096
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- Registry: GUDID
VisuBreath Ref K261633
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3047890096
- DUNS number
- 084602558
- Address
- 246 Sea View Ave, Piedmont, CA, 94610
Frequently asked questions
How many devices does Affirm Medical Technologies II, LLC have in the registry?
The registry currently lists 2 devices for Affirm Medical Technologies II, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Affirm Medical Technologies II, LLC's devices?
Among its 2 most recently registered devices, Affirm Medical Technologies II, LLC has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Affirm Medical Technologies II, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Affirm Medical Technologies II, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Affirm Medical Technologies II, LLC in the registry?
The most recently registered devices listed for Affirm Medical Technologies II, LLC include Visubreath Sticker and VisuBreath.