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
1675130510
Device Listing 1675130510
Listing Summary
#
Listing key
1675130510
Premarket submission
K905408
Device
NEXUS ACETABULAR CUP
Applicant
Dow Corning Wright
Product code
JDI
Decision date
1991-03-01
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
163593
3010536692
3010536692
MICROPORT ORTHOPEDICS INC.
1
Y
2026-01-01
5677 AIRLINE RD Arlington TN US 38002