Numotech, Inc.
United StatesFDA applicant, unverified FDA FEI 1000518730
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Numotech, Inc. makes
Numotech, Inc. manufactures non-powered hyperbaric chambers designed for extremity oxygenation therapy, as well as wound care systems like the TOTAL CONTACT SEAT RIPPLE SYSTEM. Their product line includes the Numobag Kit and standalone NUMOBAG devices, which are intended for medical applications requiring controlled oxygen delivery or pressure therapy.
The company’s devices are classified under FDA Class II regulations and are listed under the 510(k) and UDI programs. These products are registered in the United States, where Numotech, Inc. is based.
Catalogue
- Registry: GUDID
Total Contact Seat Ripple System Ref K943433
Regimes: 510(k) Registry: 510(k)Numobag Ref K981949
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000518730
- DUNS number
- 193561185
- Address
- 9420 RESEDA BLVD., SUITE 504, Northridge, CA, 91324
- [email protected]
- Phone
- 877-686-6832
Frequently asked questions
How many devices does Numotech, Inc. have in the registry?
The registry currently lists 3 devices for Numotech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Numotech, Inc.'s devices?
Among its 3 most recently registered devices, Numotech, Inc. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Numotech, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Numotech, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Numotech, Inc. in the registry?
The most recently registered devices listed for Numotech, Inc. include Numobag Kit NBC952, TOTAL CONTACT SEAT RIPPLE SYSTEM and NUMOBAG.