Inogen, Inc. FDA Approvals

0 new drug approvals and 2 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
SIMEOX 200 Airway Clearance Device510(k)Dec 23, 2024Anesthesiology	Anesthesiology	510(k)Substantially Equivalent (Traditional)	Dec 23, 2024
Inogen Rove 6510(k)Jun 30, 2023Anesthesiology	Anesthesiology	510(k)Substantially Equivalent (Traditional)	Jun 30, 2023