FDA.reportPublic FDA data

GREINER BIO-ONE NORTH AMERICA, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
11252303001451379GREINER BIO-ONE NORTH AMERICA, INC.1Y2026-01-014238 Capital Dr MONROE NC US 28110

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
94951375178204K983952GREINER VACUETTE BLOOD COLLECTION TUBEJKA1998-12-28
94951223658672K974873VACUETTE (MULTI-USE HOLDER)JKA1998-02-05
94951339232951K971236GREINER VACUETTE BLOOD COLLECTION TUBEJKA1997-05-12
94951652713450K971221GREINER VACUETTE BLOOD COLLECTION TUBEGIM1997-05-02
94951563796873K960860GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3JKA1996-09-05
94951139451925K960858GREINER VACUTTE BLOOD COLLECTION TUBE W/ CLOT ACTIVATOR & GEL SEPARATORJKA1996-08-30
94951342033708K960857GREINER VACUETTE BLOOD COLLECTION TUBE W/LITHIUM HEPARIN & GEL SEPARATORJKA1996-08-30
94951966600887K042927VACUETTE EDTA K3 EVACUATED BLOOD COLLECTION TUBESPJE2005-04-15
94951375765896K033478VACUETTE QUICKSHIELD SAFETY TUBE HOLDERFMI2003-12-29
94951714791535K023971VACUETTE TRACE ELEMENTS TUBESJKA2003-01-27
94951171310152K014104VACUETTE EDTA K2 TUBESPJE2002-02-01
94951059408061K012043VACUETTE EDTA K2 GEL TUBESPJE2001-09-24
94951929858638K011699VACUETTE EVACUATED BLOOD COLLECTION TUBESJKA2001-06-28
94951558005756BK050028
94951605384559BK050026
94951604511089BK040066
94951210609132BK040018
94951737888351BK040018
94951671016243BK030032
94951178523618BK030001
94952059825917
94952039442047

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
JKA82003-01-27
PJE32005-04-15
FMI12003-12-29
GIM11997-05-02

PMN#