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

FDA 510(k) Number Submission Date Device Name Applicant
K233123 09/27/2023 SILKRO Hironic Co., Ltd.
K241099 04/22/2024 Plasonic (Plasonic) Hironic Co., Ltd.
K173676 11/30/2017 A-FIT HIRONIC Co., Ltd.
K201773 06/29/2020 PICOHI Hironic Co., Ltd.


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