Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
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FDA Recall
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Z-1235-2016 - KAMRA Inlay, ACI 7000 Corneal Inlay, Part No. 76195-01 and 76195-10 (OUS) Labeling: The KAMRA inlay is indicated for the improvement of near visual acuity in one eye (usually the non-dominant eye) ... | 2 | 03/24/2016 | AcuFocus, Inc. |
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