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
1741036400
Device Listing 1741036400
Listing Summary
#
Listing key
1741036400
Premarket submission
K122440
Device
RESTORELLE L
Applicant
Coloplast Corp.
Product code
OTO
Decision date
2012-11-19
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
9077
2125050
2125050
COLOPLAST MANUFACTURING US, LLC
1
Y
2026-01-01
1601 W River Rd N MINNEAPOLIS MN US 55411