Acuitive Technologies, Inc. FDA Approvals

0 new drug approvals and 6 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
Citrepore510(k)Nov 6, 2024Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Nov 6, 2024
CITRELOCK® DUO510(k)Sep 20, 2023Orthopedic	Orthopedic	510(k)Substantially Equivalent (Special)	Sep 20, 2023
Citregen Tendon Interference Screw (TIS), Citrelock Tendon Fixation Device, Citrespline and Citrelock ACL Implants510(k)Feb 14, 2023Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Feb 14, 2023
Citregen Tendon Interference Screw, Citrelock, Citrefix, Citrespline ACL, and Citrelock ACL510(k)Nov 4, 2022Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Nov 4, 2022
CITRESPLINE and CITRELOCK ACL Implants510(k)Feb 24, 2021Orthopedic	Orthopedic	510(k)Substantially Equivalent (Special)	Feb 24, 2021
The Citrefix Knotless Suture Anchor510(k)Feb 5, 2021Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Feb 5, 2021