FDA 510(k) Applications Submitted by Ossvis Co., Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K242703 09/09/2024 LW Pre-milled Abutment Ossvis Co., Ltd.
K233167 09/27/2023 LW Implant System û Abutment Ossvis Co., Ltd.
K233808 11/30/2023 LW Narrow Implant System Ossvis Co., Ltd.
K242379 08/12/2024 LL Implant System Ossvis Co., Ltd.
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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