Class Class II

Augmented Gingival Matrix (K250512)

K250512 2025-12-05 Traditional
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Description

Augmented Gingival Matrix by Neo Modulus (Suzhou) Medical Sci-Tech Co., Ltd., an FDA 510(k) cleared dental device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250512
Clearance Date2025-12-05
Clearance TypeTraditional
Product CodeNPL
Regulation Number872.3930

Categories

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