Tekia, Inc.

FDA Regulatory Profile

Summary

Total Recalls
2
510(k) Clearances
0
Inspections
1
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-0694-2020Class IITEKIA Model 872 Single Piece Hydrophilic Acrylic Intraocular Lenses, Diopter 15.0, Sterile. The firNovember 9, 2018
Z-0237-2016Class IITEKIA Single Piece Hydrophilic Acrylic Intraocular Lenses, Model 811September 29, 2015