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
1279413707
Device Listing 1279413707
Listing Summary
#
Listing key
1279413707
Premarket submission
K141676
Device
RENOVIS SURGICAL POROUS ACETABULAR CUP SYSTEM
Applicant
Renovis Surgical Technologies, Inc.
Product code
LPH
Decision date
2014-11-04
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
227728
3015398319
3007932279
Kyocera Medical Technologies, Inc.
1
Y
2026-01-01
1289 Bryn Mawr Ave Ste A Redlands CA US 92374