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Meticuly Co., Ltd.

FDA Regulatory Profile

Meticuly Co., Ltd. has 0 FDA recalls, 0 inspections, 4 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Jul 25, 2026

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances4Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent 510(k) Clearances

K-NumberDeviceDate
K253206METICULY Patient-specific CMF solutionJul 25, 2026
K252958METICULY Patient-specific titanium mesh implantJan 14, 2026
K232889METICULY Patient-specific titanium maxillofacial mesh implantApr 30, 2024
K210099Meticuly Patient-Specific Titanium Mesh ImplantDec 21, 2021

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.