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
1115319676
Device Listing 1115319676
Listing Summary
#
Listing key
1115319676
Premarket submission
K130580
Device
RETRACTION PASTE
Applicant
Dmg USA, Inc.
Product code
MVL
Decision date
2014-02-25
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
73101
3006694515
3006694515
Pamela Papineau
1
N
2026-01-01
5 WHITCOMB AVENUE Ayer MA US 01432