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U.S. Department of Health and Human Services

Medical Device Recalls

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1 result found
510(K) Number: K052997
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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IMPLANT,1-PC,ANG,3.0X10MM, REF ZOP30A10; IMPLANT, 1-PC, ANG, 3.0X11.5MM, REF ZOP30A11; IMPLANT... 2 09/22/2017 Zimmer Dental Inc
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