Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K173402 |
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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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DRW-0739-01:Gen 2 Anterior Chairside Splint LRUL (lower right-upper left); accessories to the parent... | 2 | 01/26/2021 | Neocis, Inc. |
DRW-0742-01: Gen 2 Anterior Chairside Splint LLUR (lower left-upper right) - Product Usage: intended... | 2 | 07/16/2020 | Neocis Inc. |
DRW-0739-01: Gen 2 Posterior Chairside Splint LLUR (lower left-upper right) - Product Usage: intende... | 2 | 07/16/2020 | Neocis Inc. |
DRW-0739-02: Gen 2 Posterior Chairside Splint LRUL (lower right-upper left) - Product Usage: intende... | 2 | 07/16/2020 | Neocis Inc. |
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