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
2037089835
Device Listing 2037089835
Listing Summary
#
Listing key
2037089835
Premarket submission
K253586
Device
RM Electrode (RMH 25-01)
Applicant
Retmap, Inc.
Product code
HLZ
Decision date
2026-04-01
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
332965
3033274216
3033274216
RETMAP, INC.
1
N
2026-01-01
832 W Superior St # 202e Chicago IL US 60642