Tekia, Inc.
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| TEKIA Single Piece Hydrophilic Acrylic Intraocular Lenses, Model 811 recall (Z-0237-2016) | Tekia, Inc. | 2015-11-06 |
| TEKLENS II (TEKIA label) and Polylens A60 (Polytech label) Model 614, intraocular lens (IO recall (Z-1311-06) | Tekia Inc | 2006-08-02 |
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Every clearance here is in the API, with alerts when new ones post.