Greiner Bio-One North America, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Greiner Bio-One North America, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VACUETTE® QUICKSHIELD Complete (Plus)
10
Total
10
Cleared
0
Denied
Greiner Bio-One North America, Inc. has 10 FDA 510(k) cleared medical devices. Based in Baldwin, US.
Latest FDA clearance: Jul 2024. Active since 2006. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Greiner Bio-One North America, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Greiner Bio-One North America, Inc.
10 devices
Cleared
Jul 19, 2024
VACUETTE® QUICKSHIELD Complete (Plus)
General Hospital
214d
Cleared
Jan 10, 2013
BLOOD CULTURE HOLDER
Chemistry
128d
Cleared
Jul 25, 2012
SAFETY INFUSION SET
General Hospital
26d
Cleared
Feb 17, 2012
VACUETTE QUICKSHIELD WITH SNAPPY TUBE HOLDER
General Hospital
81d
Cleared
Nov 09, 2010
VACUETTE BLOOD COLLECTION TUBE WITH LITHIUM HEPARIN AND GEL SEPARATOR
Chemistry
26d
Cleared
Oct 15, 2010
VACUETTE QUICKSHIELD WITH SNAPPY TUDE HOLDER
General Hospital
21d
Cleared
Dec 16, 2008
VACUETTE BLOOD COLLECTION TUBE WITH CLOT ACTIVATOR AND GEL SEPARATOR
Chemistry
162d
Cleared
Sep 14, 2007
GREINER VACUETTE QUICKSHIELD COMPLETE
General Hospital
25d
Cleared
Jul 10, 2007
MINICOLLECT CAPILLARY BLOOD COLLECTION TUBES
Hematology
245d
Cleared
Aug 14, 2006
VACUETTE VISIO PLUS BLOOD COLLECTION NEEDLES
General Hospital
76d