Medical Device Recalls
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1 result found
510(K) Number: K183475 |
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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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| Osstem Dental X-Ray System T1. Product Model Numbers T1-C and T1-CS. | 2 | 11/05/2025 |
FEI # 3003394081 OSSTEM Implant Co., Ltd. |
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