Medical Device Recalls
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1 result found
510(K) Number: K183598 |
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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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| KeyPrint Soft- bottle, 32.5 oz (1kg). Resin for the fabrication of orthodontic and dental appliances... | 2 | 08/24/2021 |
FEI # 1000121052 Straumann USA LLC |
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