3 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Recall
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TEKIA Model 872 Single Piece Hydrophilic Acrylic Intraocular Lenses, Diopter 15.0, Sterile. The firm name on the label is TEKIA, INC., Irvine, CA.
FDA Recall
Terminated
·Tekia, Inc.·Product code HQL·November 9, 2018
TEKIA Single Piece Hydrophilic Acrylic Intraocular Lenses, Model 811
FDA Recall
Terminated
·Tekia, Inc.·Product code HQL·September 29, 2015
TEKLENS II (TEKIA label) and Polylens A60 (Polytech label) Model 614, intraocular lens (IOL)
FDA Recall
Terminated
·Tekia Inc·Product code HQL·July 2, 2004