Class Class II

Genesis ACTIVE Implant System (K223814)

K223814 2023-05-25 Traditional
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Description

Genesis ACTIVE Implant System by Keystone Dental, Inc. — FDA 510(k) cleared dental device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223814
Clearance Date2023-05-25
Clearance TypeTraditional
Product CodeDZE
Regulation Number872.3640

Categories

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