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
1765397469
Device Listing 1765397469
Listing Summary
#
Listing key
1765397469
Premarket submission
K093676
Device
OMNITECH LARGE, TRIMED COMPRESSION SCREW
Applicant
TriMed, Inc.
Product code
HWC
Decision date
2010-03-17
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
17217
2031009
3001236812
TRIMED, INC.
1
Y
2026-01-01
27533 Avenue Hopkins Santa Clarita CA US 91355