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
1790961557
Device Listing 1790961557
Listing Summary
#
Listing key
1790961557
Premarket submission
K213116
Device
Everyway Incontinence Stimulation System
Applicant
Everyway Medical Instruments Co.,Ltd
Product code
KPI
Decision date
2021-12-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
317489
3027329006
3027329006
AXION USA LLC
1
Y
2026-01-01
120 Raskulinecz Rd Carteret NJ US 07008