The New Era in Bone Growth Stimulation

Introducing the ActaStim®-S System

Small Device. Big Compliance Impact.
Ready to experience the difference firsthand?

The ActaStim bone growth stimulation system for patients recovering from spine fusion

Fill out the form to get a personalized demo and see how it can benefit your practice.

*Required fields

Empowering Patient Recovery with Advanced Patient Insights, Continuous Wearability and VIP Care

Spine Surgery has significantly advanced over the last 20 years, spinal bone growth stimulators have not – until now.

The first major breakthrough in non-invasive spinal fusion bone growth stimulation in almost 20 years, ActaStim®-S is specifically designed to enhance patient compliance and improve fusion success with clinically proven therapy. It’s the only system that supports continuous wearability and automatically tracks wear time and relative activity levels, alongside pain scores, to better support a successful healing journey.

Two images showing a healthcare professional viewing the ActaStim portal on her laptop and a middle-aged male ActaStim user consulting his spine surgeon.

Built on Trusted Technology

0 %

increase in fusion success, regardless of the type of fusion1

0 x

more likely to have a successful outcome2

0 %

reduction in
failure rates1

reduction in failure rates2

Patient Insights

Real-Time recovery progress and metrics, actionable patient insights and preset alerts

A female patient updating her pain levels in the companion app for the ActaStim bone growth stimulation system
A male patient placing the ActaStim bone growth stimulation system in his pocket

Comfortable, Discreet, Portable – Wearability Leads to Better Fusion3,4

Designed for continuous wear with a user-friendly interface app

VIP Customer Care

Our goal is to unburden you and your staff, keeping your patient our focus with
  • Insurance navigation assistance
  • Hands on patient training
  • VIP patient support
  • Dedicated, U.S. technical support staff
  • Patient tools and resources
Smiling middle-aged female ActaStim user consulting her spine surgeon

References: 

1. Goodwin CB, Brighton CT, Guyer RD, Johnson JR, Light KI, Yuan HA. A double-blind study of capacitively coupled electrical stimulation as an adjunct to lumbar spinal fusions. Spine (Phila Pa 1976). 1999;24(13):1349-1357. doi:10.1097/00007632-199907010-00013

2. U.S. Food and Drug Administration. (2020). PMA P190030: FDA Summary of Safety and Effectiveness Data.

3. Brighton CT, Wang W, Seldes R, Zhang G, Pollack SR. Signal transduction in electrically stimulated bone cells. J Bone Joint Surg Am. 2001;83(10):1514-1523. doi:10.2106/00004623-200110000-00009

4. Mooney V. A randomized double-blind prospective study of the efficacy of pulsed electromagnetic fields for interbody lumbar fusions. Spine (Phila Pa 1976). 1990;15(7):708-712. doi:10.1097/00007632-199007000-00016

Indications for Use

The ActaStim®-S Spine Fusion Stimulator is a noninvasive bone growth stimulator indicated as an adjunct electrical treatment to primary lumbar spinal fusion surgery for one or two levels. The device is Rx only, and intended for single patient use in adult patients only.

ActaStim® (spine fusion stimulator) or its use is covered by one or more of the following U.S. patents: 11,395,919; 11,426,574;11,717,685;11,759,637;11,857,785. Additional U.S. and foreign patents pending. 2471-WEB-003 Rev. B