Welch Allyn, Inc. 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
Welch Allyn Connex® 360 (Multiple)510(k)Jul 13, 2025	—	510(k)Substantially Equivalent (Traditional)	Jul 13, 2025
Welch Allyn Connex® Spot Monitor; 901058 Vital Signs Monitor Core (CSM)510(k)Dec 20, 2024Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Dec 20, 2024
iExaminer System with Panoptic Plus510(k)Mar 15, 2023Ophthalmic	Ophthalmic	510(k)Substantially Equivalent (Traditional)	Mar 15, 2023
Welch Allyn Connex Central Station510(k)Oct 28, 2022Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Oct 28, 2022