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
1670500387
Device Listing 1670500387
Listing Summary
#
Listing key
1670500387
Premarket submission
K110037
Device
PALAXPRESS ULTRA POWDER (PINK); PALAXPRESS ULTRA LIQUID
Applicant
Heraeus Kulzer, LLC
Product code
EBI
Decision date
2011-04-29
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
21764
9610902
3002807166
KULZER GMBH
1
N
2026-01-01
PHILIPP-REIS-STRASSE 8/13 WEHRHEIM Hesse DE D-61273
176134
3011203516
3011203516
David Vincent
1
N
2026-01-01
4315 S Lafayette Blvd South Bend IN US 46614