FDA.reportPublic FDA data

CENTESE, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30174357053017435705CENTESE, INC.1N2026-01-014156 S 52nd St Omaha NE US 68117

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00860000436403Thoraguard - Thoraguard Chest Tube Kit, 20 Fr888-220-0040customerservice@centese.com
00860000436410Thoraguard - Thoraguard Drainage Kit888-220-0040customerservice@centese.com
00860000436427Thoraguard - Thoraguard Control Module888-220-0040customerservice@centese.com
00860000436441Thoraguard - Thoraguard Chest Tube Kit, 28 Fr888-220-0040customerservice@centese.com
10860000436400Thoraguard - Thoraguard Chest Tube Kit, 20 Fr888-220-0040customerservice@centese.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2793472050399458K181667Thoraguard SystemBTA2018-11-29
2793471965240784

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
BTA12018-11-29

PMN#

GUDID#