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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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