Medexel Co.,Ltd

FDA Regulatory Profile

Medexel Co.,Ltd appears in FDA public data with 0 recalls, 3 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 15, 2024.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K231856TopFine® LDS (Low Dead Space) Syringe (2 models (TS-LDS2334, TS-LDS2534))March 15, 2024
K172095AutokeeperJuly 24, 2018
K152410Top Fine Pen NeedleFebruary 2, 2016