# TRUERELIEF

FEI: 3015550326
Status: Active
Establishment types: Develop Specifications But Do Not Manufacture At This Facility; Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: TrueRelief (#10060510)

Address: 100 Wilshire Boulevard, Suite 700, Santa Monica, CA, US



## Products

Total registered: 1
Top product codes: GZJ
Regulation §: 882.5890

Proprietary names: TRUERELIEF, Model 1250 TRUERELIEF Device, TRUERELIEF 1250, TRUERELIEF Secondary Probe, Model P12S Secondary Probe, TRUERELIEF Probe Tips, Probe Tips, Model P12T10 Probe Tips, TRUERELIEF Primary Probe, Model P12P Primary Probe, TRUERELIEF Kit, Model TR1250C TRUERELIEF Kit, TRUERELIEF Power Cord with Wall Wart, Model WW12 Power Cord with Wall Wart

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223015550326%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3015550326