Guangzhou Pluslife Biotech Co., Ltd.

FDA Regulatory Profile

Summary

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

Recent Recalls

NumberClassProductDate
Z-1978-2025Class IIBrand Name: MiniDock Product Name: Integrated Nucleic Acid Testing Device Model/Catalog Number: PMJanuary 24, 2025
Z-1979-2025Class IIBrand Name: Pluslife SARS-CoV-2 Card Product Name: SARS-CoV-2 Nucleic Acid Testing Card Model/CataJanuary 24, 2025