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
1018014393
Device Listing 1018014393
Listing Summary
#
Listing key
1018014393
Premarket submission
K112193
Device
ARROW REVERSE SHOULDER SYSTEM
Applicant
Fournitures Hospitalieres Industrie
Product code
PHX
Decision date
2012-07-12
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
16400
3003898228
3003898228
FH INDUSTRIE
1
N
2026-01-01
ZI DE KERNEVEZ-6 RUE NOBEL QUIMPER Finistere FR 29000