Class Class II

Geistlich Mucograft® /Geistlich Mucograft® Seal; Geistlich Fibro-Gide® (K252253)

K252253 2025-11-25 Traditional
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Description

Geistlich Mucograft® /Geistlich Mucograft® Seal; Geistlich Fibro-Gide® by Geistlich Pharma AG, an FDA 510(k) cleared dental device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252253
Clearance Date2025-11-25
Clearance TypeTraditional
Product CodeNPL
Regulation Number872.3930

Categories

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