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Meticuly Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K252958METICULY Patient-specific titanium mesh implantJanuary 14, 2026
K232889METICULY Patient-specific titanium maxillofacial mesh implantApril 30, 2024
K210099Meticuly Patient-Specific Titanium Mesh ImplantDecember 21, 2021