Lucero Medical LLC

FDA Regulatory Profile

Lucero Medical LLC appears in FDA public data with 1 recall, 3 510(k) clearances, 4 FDA inspections, and 1 compliance action on record. Its most recent recall (Z-2368-2012, Class II) was initiated on July 15, 2012. Its most recent 510(k) clearance was granted on December 16, 2020.

Summary

Total Recalls
1
510(k) Clearances
3
Inspections
4
Compliance Actions
1

Recent Recalls

NumberClassProductDate
Z-2368-2012Class IIEnduramesh Corpectomy Spacer System Product Usage: The Enduramesh is a vertebral body replacementJuly 15, 2012

Recent 510(k) Clearances

K-NumberDeviceDate
K200549Lucero Medical Cervical Cage SystemDecember 16, 2020
K122622ENDURAMESHSeptember 19, 2012
K093207ENDURAMESH, MODEL 762.XXXApril 26, 2010