FDA 510(k) Applications Submitted by Ossvis Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K231079 | 04/17/2023 | LW Retraction Cap | Ossvis Co., Ltd. |
| K231235 | 04/28/2023 | LW UCLA Abutment | Ossvis Co., Ltd. |
| K223924 | 12/30/2022 | LW Implant System | Ossvis Co., Ltd. |
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