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

FDA 510(k) Number Submission Date Device Name Applicant
K151232 05/08/2015 VIKINI Diode Laser System ILOODA CO., LTD
K160312 02/05/2016 FRAXIS DUO ILOODA CO., LTD
K211000 04/02/2021 ACUTRON ILOODA Co., Ltd
K212561 08/13/2021 MTX-C1 ILOODA Co., Ltd


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