Tekia, Inc.
Tekia, Inc. appears in FDA public data with 2 recalls, 0 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-0694-2020, Class II) was initiated on November 9, 2018.
Summary
- Total Recalls
- 2
- 510(k) Clearances
- 0
- Inspections
- 1
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-0694-2020 | Class II | TEKIA Model 872 Single Piece Hydrophilic Acrylic Intraocular Lenses, Diopter 15.0, Sterile. The fir | November 9, 2018 |
| Z-0237-2016 | Class II | TEKIA Single Piece Hydrophilic Acrylic Intraocular Lenses, Model 811 | September 29, 2015 |