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
1400879499
Device Listing 1400879499
Listing Summary
#
Listing key
1400879499
Premarket submission
K151542
Device
A-Oss
Applicant
Hiossen, Inc.
Product code
NPM
Decision date
2016-08-03
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