PROVIDENCE MEDICAL TECHNOLOGIES

FDA Regulatory Profile

PROVIDENCE MEDICAL TECHNOLOGIES appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2428-2020, Class II) was initiated on March 29, 2019.

Summary

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

Recent Recalls

NumberClassProductDate
Z-2428-2020Class IIAlly Bone Screw - Product Usage:Bone Screws are indicated for use in bone reconstruction, osteotomy,March 29, 2019