Meticuly Co., Ltd. FDA Approvals

0 new drug approvals and 4 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
METICULY Patient-specific CMF solution510(k)Jul 25, 2026Dental	Dental	510(k)Substantially Equivalent (Traditional)	Jul 25, 2026
METICULY Patient-specific titanium mesh implant510(k)Jan 14, 2026Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	Jan 14, 2026
METICULY Patient-specific titanium maxillofacial mesh implant510(k)Apr 30, 2024Dental	Dental	510(k)Substantially Equivalent (Traditional)	Apr 30, 2024
Meticuly Patient-Specific Titanium Mesh Implant510(k)Dec 21, 2021Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	Dec 21, 2021