FDA 510(k) Applications Submitted by Incore Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K220846 | 03/23/2022 | CORE-SNARE | Incore Co., Ltd. |
| K221054 | 04/11/2022 | CORE-INJECTOR | Incore Co., Ltd. |
| K211148 | 04/19/2021 | CORE-Trocar | Incore CO., LTD. |
| K213338 | 10/07/2021 | CORE-CLIP | Incore Co., Ltd. |
| K220081 | 01/10/2022 | CORE-SPORT | Incore Co., Ltd. |
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