Myohealth Technologies, LLC
United Statesfrom the FDA registration address FDA establishment FEI 3030686055
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Myoaligner Appliance Ref K230548
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3030686055
- Address
- 13765 NW Cornell Rd, Portland, OR, 97229
Frequently asked questions
How many devices does MYOHEALTH TECHNOLOGIES, LLC have in the registry?
The registry currently lists 2 devices for MYOHEALTH TECHNOLOGIES, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list MYOHEALTH TECHNOLOGIES, LLC's devices?
Among its 2 most recently registered devices, MYOHEALTH TECHNOLOGIES, 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 are the newest devices from MYOHEALTH TECHNOLOGIES, LLC in the registry?
The most recently registered devices listed for MYOHEALTH TECHNOLOGIES, LLC include Myoaligner® MYO-001 and Myoaligner Appliance.