Manteia Technologies Co., Ltd. FDA Approvals

0 new drug approvals and 7 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
MRIA Radiation Therapy Information System (MRIA)510(k)Aug 26, 2026Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Aug 26, 2026
AccuContour 4.0510(k)Jan 23, 2026Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Jan 23, 2026
ARTAssistant510(k)Dec 5, 2025Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Dec 5, 2025
AccuCheck510(k)Oct 24, 2025Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Oct 24, 2025
AccuCheck510(k)Jul 20, 2023Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Jul 20, 2023
MOZI TPS510(k)Jul 10, 2023Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Jul 10, 2023
AccuContour510(k)Mar 9, 2023Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Mar 9, 2023