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FDA 510(k) Applications Submitted by Incore Co., Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K220846
03/23/2022
CORE-SNARE
Incore Co., Ltd.
K221054
04/11/2022
CORE-INJECTOR
Incore Co., Ltd.
K211148
04/19/2021
CORE-Trocar
Incore CO., LTD.
K213338
10/07/2021
CORE-CLIP
Incore Co., Ltd.
K220081
01/10/2022
CORE-SPORT
Incore Co., Ltd.
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