Medical Device Recalls
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1 result found
510(K) Number: K103087 |
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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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| RENOVIX Guided Healing Collagen Membrane Intended for use in oral surgical procedures. | 2 | 01/27/2017 |
FEI # 3007702492 Biom'up |
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