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
1786825858
Device Listing 1786825858
Listing Summary
#
Listing key
1786825858
Premarket submission
K101044
Device
RETRIEVE IMPLANT CEMENT
Applicant
Parkell, Inc.
Product code
EMA
Decision date
2010-06-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
199606
2411797
2411797
PARKELL, INC.
1
Y
2026-01-01
300 EXECUTIVE DR. EDGEWOOD NY US 11717