3-D Matrix Europe SAS 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
PuraStat510(k)Jan 7, 2026	—	510(k)Substantially Equivalent (Special)	Jan 7, 2026
PuraStat510(k)Jan 7, 2026General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Special)	Jan 7, 2026
PuraStat510(k)Jan 15, 2025	—	510(k)Substantially Equivalent (Traditional)	Jan 15, 2025
PuraStat510(k)Oct 22, 2024General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Traditional)	Oct 22, 2024