Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1016278107
Device Listing 1016278107
Listing Summary
#
Listing key
1016278107
Premarket submission
K210278
Device
Titan SGS
Applicant
Standard Bariatrics
Product code
GDW
Decision date
2021-04-28
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
152269
3010041511
3010041511
Teleflex LLC (NADC)
1
Y
2027-01-01
11245 N Distribution Cove Olive Branch MS US 38654
175463
3011137372
3005747797
Teleflex Medical LLC
1
Y
2027-01-01
3015 Carrington Mill Blvd Morrisville NC US 27560
313340
3012481535
3012481535
Teleflex Medical Inc.
1
N
2026-01-01
4300 Glendale Milford Road Cincinnati OH US 45242