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
1773951462
Device Listing 1773951462
Listing Summary
#
Listing key
1773951462
Premarket submission
K041960
Device
COMPOSITE/COMPOMER REPAIR KIT
Applicant
Dmg USA, Inc.
Product code
KLE
Decision date
2004-08-30
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
13630
8044164
3004150030
Pamela Papineau
1
N
2026-01-01
5 WHITCOMB AVENUE Ayer MA US 01432