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
1217089489
Device Listing 1217089489
Listing Summary
#
Listing key
1217089489
Premarket submission
K220823
Device
Preat Abutments
Applicant
Preat Corporation
Product code
NHA
Decision date
2022-10-26
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
21405
2087481
1000253567
TRIDENT LAB INC.
1
Y
2026-01-01
12000 AVIATION BLVD. HAWTHORNE CA US 90250