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
1343169939
Device Listing 1343169939
Listing Summary
#
Listing key
1343169939
Premarket submission
K031664
Device
ELEMENTS OBTURATION UNIT
Applicant
Sybron Endo/Analytic
Product code
EKR
Decision date
2004-04-28
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
16974
2016150
2016150
Ormco Corporation, also trading as SybronEndo
1
Y
2020-04-25
1332 S Lone Hill Ave Glendora CA US 91740
16973
2024312
2024312
Kerr Corporation
1
Y
2026-01-01
1717 W Collins Ave ORANGE CA US 92867
16971
9680845
3000368601
Procoro Herrera
1
N
2026-01-01
200 S. Kraemer Blvd. Brea CA US 92821