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
1059701648
Device Listing 1059701648
Listing Summary
#
Listing key
1059701648
Premarket submission
K061983
Device
STIMUPLEX PEN
Applicant
Stockert GmbH
Product code
BXN
Decision date
2006-11-21
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
9226
9610825
3002806469
Kamaal Anas
1
N
2026-01-01
824 Twelfth Avenue Bethlehem PA US 18018
130731
3009224460
3009224460
REBECCA - STOLARICK
1
N
2020-04-25
901 Marcon Blvd Allentown PA US 18109