Medical Device Recalls
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1 result found
510(K) Number: K172918 |
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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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| DEXIS Titanium Intraoral Sensor Product Usage: The DEXIS Titanium Intraoral Sensor is a USB-driv... | 2 | 05/21/2019 |
FEI # 1017522 KaVo Dental Technologies LLC |
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