Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1686257359
Device Listing 1686257359
Listing Summary
#
Listing key
1686257359
Premarket submission
K202186
Device
TrueRelief Device
Applicant
Truerelief
Product code
GZJ
Decision date
2021-03-23
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
230032
3015550326
3015550326
TRUERELIEF
1
N
2026-01-01
100 Wilshire Boulevard Suite 700 Santa Monica CA US 90401