Medical Device Recalls
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1 result found
510(K) Number: K895886 |
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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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| BioPro Endo Head (Metal uni-polar, 38-55) Product Number/Description 10179 ENDO MD 38 10180 E... | 2 | 10/14/2025 | BioPro, Inc. |
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