Medical Device Recalls
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1 result found
510(K) Number: K922499 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Avex CX Suite, Avex CX 0.22 UL4,5 HK REF #224-017, Product Usage: Avex CX ceramic brackets a... | 3 | 02/22/2013 | Ultradent Products, Inc. |
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