Greiner Bio-One Na, Inc.

FDA Regulatory Profile

Greiner Bio-One Na, Inc. has 0 FDA recalls, 0 inspections, 5 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Jan 25, 2019

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances5Oct 4, 2026Not statedCurrent
Inspections0Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K182078MiniCollect K2E K2EDTA TubesJan 25, 2019
K180545VACUETTE SAFELINK Holder with male luer lockMay 21, 2018
K173757VACUETTE EVOPROTECT Safety Blood Collection / Infusion SetApr 19, 2018
K163436Greiner Vacuette Urine Count and Culture, Mannitol tubeMar 6, 2017
K160532Greiner HoldexNov 3, 2016