Shandong Lianfa Medical Plastic Products Co. , Ltd. 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
Lancing System, Sterile Lancet for Single Use, Lancing Device510(k)Nov 30, 2022General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Traditional)	Nov 30, 2022
Lianfa Safety Lancet (Five Models: NPA, PA, PA2, TPA, and APA)510(k)Oct 3, 2022General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Traditional)	Oct 3, 2022