Truerelief
United Statesfrom the FDA registration address FDA FEI 3015550326
Truerelief is a medical device manufacturer, with 7 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 12 Nov 2026.
- Devices
- 7
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 6
- FDA 510(k) 1
- Device classes
- FDA Class II 7
- Identifiers
- FDA FEI 3015550326
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
TrueRelief Device Ref K202186
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3015550326
- Address
- 9375 E Shea Blvd Ste 250c, Scottsdale, AZ, 85260
Frequently asked questions
How many devices does Truerelief have in the registry?
The registry currently lists 7 devices for Truerelief. Devices recorded under merged duplicate company entries are counted once.
Which registries list Truerelief's devices?
Among its 7 most recently registered devices, Truerelief has devices listed in FDA 510(k) (1 device) and FDA GUDID (6 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Truerelief's devices fall under?
Among its 7 most recently registered devices, the classes recorded for Truerelief's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Truerelief in the registry?
The most recently registered devices listed for Truerelief include TrueRelief P12P, TrueRelief WW12, TrueRelief P12T10 and TrueRelief 1250.