Home / Companies / Alexotek Co.

Alexotek Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K881789MINILINE BRACKETJune 1, 1988
K834446ALEXOTEK LINGUAL TUBESApril 5, 1984
K834392LABIAL CUSPID TUBEFebruary 28, 1984
K834272ALEXOLOK BRACKETFebruary 3, 1984