Class Class II

Primevision 3D (K253959)

K253959 2026-02-05 Traditional
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Description

Primevision 3D by Dentsply Sirona, an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253959
Clearance Date2026-02-05
Clearance TypeTraditional
Product CodeOAS
Regulation Number892.1750

Categories

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