Meticuly Co., Ltd.

FDA Regulatory Profile

Meticuly Co., Ltd. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 25, 2026.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253206METICULY Patient-specific CMF solutionJuly 25, 2026
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