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
1528651908
Device Listing 1528651908
Listing Summary
#
Listing key
1528651908
Premarket submission
K150454
Device
Acryfree Denture Base Material and Biosens Denture Base Material
Applicant
Perflex
Product code
EBI
Decision date
2015-05-26
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
177939
3011532731
3011532731
PERFLEX LTD
1
N
2026-01-01
4 Hamelacha str. New Ind. Area Netanya Central IL 4250539