CORENTEC CO., LTD
3 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| LOSPA Tibial Insert Model/Catalog Number: See below Software Version: N/A Product Descript recall (Z-1934-2024) | CORENTEC CO., LTD | 2024-05-31 |
| LOSPA Patella Component Model/Catalog Number: 01.10.9XX Software Version: N/A Product Desc recall (Z-1935-2024) | CORENTEC CO., LTD | 2024-05-31 |
| Bencox Mirabo PE Liner 36/44 Model Number: H1.L61.3644, UDI: 8806373852343 recall (Z-1454-2017) | CORENTEC CO., LTD | 2017-03-13 |
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Every clearance here is in the API, with alerts when new ones post.