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FDA 510(k) Applications Submitted by Biotem Co., Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K190641
03/13/2019
AR_N SLA Type Implant System
Biotem Co., Ltd.
K171185
04/24/2017
IR Type Implant System
Biotem Co., Ltd.
K171297
05/02/2017
AR_N Type Implant System
Biotem Co., Ltd.
K222142
07/20/2022
BR SLA Type Implant System
Biotem Co., Ltd.
K222144
07/20/2022
IR SLA Type Implant System
Biotem Co., Ltd.
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