Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-0012-2007 - Bio-Eye Hydroxyapatite (HA) Orbital Implant and Conformer, Model Number: 100020S | 3 | 10/04/2006 |
FEI # 3009688114 Integrated Orbital Implants Inc |
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