TIDI PRODUCTS

FDA Regulatory Profile

TIDI PRODUCTS appears in FDA public data with 1 recall, 3 510(k) clearances, 8 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0194-2020, Class II) was initiated on April 12, 2019. Its most recent 510(k) clearance was granted on February 18, 2014.

Summary

Total Recalls
1
510(k) Clearances
3
Inspections
8
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-0194-2020Class IIPosey Connected Twice-As-Tough CuffsApril 12, 2019

Recent 510(k) Clearances

K-NumberDeviceDate
K132953TIDISHEILDFebruary 18, 2014
K100800TIDI FACEMASKJune 14, 2010
K092580TIDI FACEMASKFebruary 23, 2010