Timpel S.A. FDA Approvals

0 new drug approvals and 3 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
Enlight 2100 (TPL-E2103-0)510(k)Sep 10, 2025Anesthesiology	Anesthesiology	510(k)Substantially Equivalent (Traditional)	Sep 10, 2025
Enlight 2100510(k)Mar 7, 2023Anesthesiology	Anesthesiology	510(k)Substantially Equivalent (Traditional)	Mar 7, 2023
Enlight 2100510(k)Jan 6, 2022Anesthesiology	Anesthesiology	510(k)Substantially Equivalent (Traditional)	Jan 6, 2022