Become a KeyLift® Distributor
We’re building the KeyLift distributor network one relationship at a time. If you believe in moving the right device to the right patient, we’d love to hear from you.
KeyLift is the only FDA-cleared expandable interlaminar stabilization device indicated through L5-S1.¹
Our distributor partners are the front line of getting it into the hands of the spine specialists who need it. We invest in our partners with hands-on clinical training, a co-branded education library, and a direct line to the founding team.
Tell us a little about your territory and we’ll be in touch.
¹ Based on FDA 510(k) database review for product code PEK. KeyLift™ K232484 indicated T1-S1; coflex® (P110008) indicated L1-L5; competing PEK devices are not expandable. Current as of June 2026.
AM01-0059