FDA 510(k) Applications Submitted by Dentis Co., Ltd
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K230126 | 01/17/2023 | Dentis s-Clean Regular Abutment | Dentis Co., Ltd |
| K222976 | 09/28/2022 | MU System | Dentis Co., Ltd |
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