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
1278458137
Device Listing 1278458137
Listing Summary
#
Listing key
1278458137
Premarket submission
K110766
Device
KOLPLUX SYSTEM
Applicant
Kolplast CI Ltda
Product code
HIB
Decision date
2011-09-15
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
13479
8044093
3005729015
Kolplast Ci Ltda
1
N
2026-01-01
Estrada Municipal Benedito De Souza #418 Bairro Da Mina Itupeva Sao Paulo BR 13299-364