Centese Inc.

FDA Regulatory Profile

Summary

Total Recalls
1
510(k) Clearances
1
Inspections
1
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-0105-2022Class IIThoraguard Chest Tube Kit, 20 FrAugust 31, 2021

Recent 510(k) Clearances

K-NumberDeviceDate
K181667Thoraguard SystemNovember 29, 2018