FDA 510(k) Applications Submitted by Corentec Co., Ltd.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K250889 |
03/25/2025 |
EXULT Knee Replacement System |
Corentec Co., Ltd. |
| K242046 |
07/12/2024 |
EXULT Knee Replacement System |
Corentec Co., Ltd. |
| K242401 |
08/13/2024 |
EXULT Knee Replacement System |
Corentec Co., Ltd. |
| K211866 |
06/16/2021 |
Bencox THR System |
Corentec Co., Ltd. |
| K212034 |
06/29/2021 |
LOSPA TKR System |
Corentec Co., Ltd. |
| K223223 |
10/17/2022 |
BENCOX Mirabo Z Cup Cortinium |
Corentec Co., Ltd. |
| K200267 |
02/03/2020 |
LOSPA« ISÖ Spinal Fixation System |
Corentec Co., Ltd. |
| K222278 |
07/29/2022 |
LOSPA TKR System Instrumentation, EXULT TKR System Instrumentation |
Corentec Co., Ltd. |
| K223828 |
12/21/2022 |
BENCOX Delta Option Heads |
Corentec Co., Ltd. |
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