Medical Device Recalls
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1 result found
510(K) Number: K180036 |
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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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| Smaxel Fractional CO2 Laser, a Class IV medical laser system. | 2 | 01/07/2025 | IDS LTD |
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