Ventris Medical FDA Approvals

0 new drug approvals and 5 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
Collagen Wound Powder510(k)Jul 2, 2026	—	510(k)Substantially Equivalent (Traditional)	Jul 2, 2026
Porous Biologic Scaffold510(k)Mar 21, 2025Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Mar 21, 2025
Porous Biologic Scaffold510(k)Dec 18, 2024Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Dec 18, 2024
Synthetic Bone Putty510(k)Mar 7, 2024Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Mar 7, 2024
Synthetic Bone Putty510(k)Sep 2, 2022Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Sep 2, 2022