Gentueri Inc

FDA Regulatory Profile

Gentueri Inc appears in FDA public data with 2 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0504-2022, Class II) was initiated on March 18, 2021.

Summary

Total Recalls
2
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-0504-2022Class IIGentueri Viral Transport Medium (VTM), Sterile, IVDMarch 18, 2021
Z-0561-2022Class IIGentueri Viral Transport Medium Kit with 8cm Breakpoint SwabJuly 6, 2020