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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K232889

METICULY Patient-specific titanium maxillofacial mesh implant · Meticuly Co., Ltd. · decided 2024-04-30 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
METICULY Patient-specific titanium maxillofacial mesh implantMF-314METICULY COMPANY LIMITEDJEY08859751213144
METICULY Patient-specific titanium maxillofacial mesh implantMF-311METICULY COMPANY LIMITEDJEY08859751213113
METICULY Patient-specific titanium maxillofacial mesh implantMF-212METICULY COMPANY LIMITEDJEY08859751212123
METICULY Patient-specific titanium maxillofacial mesh implantMF-312METICULY COMPANY LIMITEDJEY08859751213120
METICULY Patient-specific titanium maxillofacial mesh implantMF-313METICULY COMPANY LIMITEDJEY08859751213137
METICULY Patient-specific titanium maxillofacial mesh implantMF-211METICULY COMPANY LIMITEDJEY08859751212116