Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K161689 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Osstem Implant System - Abutment: ET Multi AbutmentSize: 4.8D 5.0GH - Abutment is intended for use ... | 2 | 03/05/2025 |
FEI # 3007135442 Hiossen Inc. |
| Osstem Implant System - Abutment ET Multi Abutment Size: 4.8D 3.0G/H- Abutment is intended for use ... | 2 | 03/05/2025 |
FEI # 3007135442 Hiossen Inc. |
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