Medical Device Recalls
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1 result found
510(K) Number: K021337 |
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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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| Brand Name: AART Pectoral Implant Product Name: Pectoral Implant Model/Catalog Number: 500-106-5 ... | 2 | 12/18/2025 | DSAART LLC |
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