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
1932673448
Device Listing 1932673448
Listing Summary
#
Listing key
1932673448
Premarket submission
K191751
Device
EM Provisional
Applicant
Hiossen, Inc.
Product code
DZE
Decision date
2019-12-16
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
90823
3007135442
3007135442
HIOSSEN INC.
1
N
2026-01-01
85 BEN FAIRLESS DR Fairless Hills PA US 19030