Aevumed, Inc. FDA Approvals

0 new drug approvals and 7 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
Aevumed SUPERCYNCH Button System510(k)Sep 2, 2026Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Sep 2, 2026
Aevumed FENIX Suture Anchor510(k)Mar 4, 2026Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Mar 4, 2026
Aevumed PROTEKT Suture Anchor510(k)Jan 28, 2026Orthopedic	Orthopedic	510(k)Substantially Equivalent (Special)	Jan 28, 2026
Aevumed FASE Suture Anchor510(k)Oct 21, 2025Orthopedic	Orthopedic	510(k)Substantially Equivalent (Special)	Oct 21, 2025
Aevumed PHANTOM Suture Anchors510(k)Aug 6, 2025Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Aug 6, 2025
Aevumed RAPID Suture Anchors510(k)Mar 17, 2023Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Mar 17, 2023
Aevumed PHANTOM-LP Suture Anchors510(k)Nov 28, 2022Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Nov 28, 2022