Medical Device Recalls
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1 result found
510(K) Number: K181112 |
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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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| O3D ORCHESTRATE Orthodontic Technologies User Manual and Data Processing Instructions (model prepar... | 2 | 12/06/2021 | Orchestrate Orthodontic Technologies, Inc. |
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