Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K001899 |
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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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Nexus Universal with OptiBond Universal, Universal Adhesive Resin Cement, Trial Kit, Ref # 36990 - ... | 2 | 04/29/2020 | Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical |
NX3 Try-In Gel. The product is used as a tooth shade resin material. | 2 | 09/19/2013 | Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical |
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