Class Class II

Primeprint Direct Aligner (K250739)

K250739 2025-11-07 Traditional
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Description

Primeprint Direct Aligner by Dreve Dentamid GmbH, an FDA 510(k) cleared dental device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250739
Clearance Date2025-11-07
Clearance TypeTraditional
Product CodeNXC
Regulation Number872.5470

Categories

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