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
1609004054
Device Listing 1609004054
Listing Summary
#
Listing key
1609004054
Premarket submission
K191374
Device
Revival Modular Hip Stem
Applicant
Corin U.S.A. Limited
Product code
LZO
Decision date
2019-07-22
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
194285
3007391088
3007391088
Shannon Danho
1
N
2026-01-01
480 Paramount Dr Raynham MA US 02767