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FDA 510(k) Applications Submitted by ORTHOREBIRTH CO., LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K142090
08/01/2014
REBOSSIS
ORTHOREBIRTH CO., LTD.
K170620
03/01/2017
ReBOSSIS85
ORTHOREBIRTH Co., Ltd.
K172573
08/28/2017
ReBOSSIS85
Orthorebirth Co., Ltd.
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