Shenzhen Jian Feng Electronic Technology Co., Ltd. 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
Tens & Ems Device510(k)May 9, 2023Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	May 9, 2023
TENS & EMS DEVICE (Model: FM-B2403A)510(k)Mar 8, 2022Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	Mar 8, 2022
TENS & EMS Device510(k)Mar 3, 2022Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	Mar 3, 2022
TENS & EMS Device510(k)May 19, 2021Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	May 19, 2021