Class Class II

Hi-Bond Universal (K230465)

K230465 2023-05-22 Traditional
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Description

Hi-Bond Universal by Mediclus Co., Ltd. — FDA 510(k) cleared dental device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230465
Clearance Date2023-05-22
Clearance TypeTraditional
Product CodeKLE
Regulation Number872.3200

Categories

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