Frequently Asked Questions

Everything you need to know about Spark™

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KinetiTec Spark™ | FAQ Section
About Spark™

What is KinetiTec Spark™?

Spark™ is a recumbent in-bed system that integrates strength maintenance, cardiopulmonary engagement, and objective measurement into a single device. It fills the gap between bed rest and ambulation by providing structured movement and activity data for hospitalized patients.

What does Spark™ do that other devices don't?

Spark™ is the only system that combines all three capabilities — upper and lower body resistance, cardiopulmonary engagement, and cloud-connected objective measurement — in a single lightweight, portable device that requires no cords. No competitor covers the key capabilities Spark™ delivers.

Is Spark™ an FDA-regulated device?

Yes. Spark™ is a Class I medical device under FDA product code ION, regulation code 890.5370. It is designed to support structured in-bed movement and present objective activity data.

How long does it take to set up Spark™?

Under 60 seconds. Spark™ clamps directly to any standard hospital bed frame. No tools, no technicians, no modifications.

Does Spark™ require a power source?

No. Spark™ is self-sustaining. Patient activity powers the device. No cords, no outlets, no charging required.

How much does Spark™ weigh?

Under 15 pounds. One-person carry, minimal space.
For Hospitals & Facilities

What kind of data does Spark™ capture?

Spark™ captures objective activity data from each patient session and transmits it wirelessly to the cloud. Care teams can access dashboards that support documentation, activity trending, and discharge planning workflows.

Can Spark™ connect to our EMR?

Spark's software platform is designed with EMR integration in mind. The system captures and stores data in cloud-based dashboards that can support clinical documentation workflows. Specific EMR integration details are available on request.

Does Spark™ require clinical supervision?

No. Spark™ is designed for safe self-supervised use. Patients can engage at their own pace without requiring a clinician at the point of use.

What size facilities is Spark™ designed for?

Acute care hospitals and post-acute rehabilitation facilities of all sizes. The ROI calculator on our website lets you project savings based on your specific admissions volume and average length of stay.
For Investors

Where is KinetiTec™ in its development?

KinetiTec™ is raising a $1M pre-seed round. $420K raised to date with Boomerang Ventures as lead investor. 3 live deployments, 20 institutions in active discussions, 10 pilot agreements, and 3 IRB protocols.

How can I request investor materials?

Contact Kathy Phlegar directly at hello@kinetitec.com or use the Investor Information page to request the pitch deck and supporting materials.
For Clinicians & Researchers

Is there published research on Spark™?

Yes, our published research includes:

Development and Internal Validation of the Immobility Harm Risk Score for Predicting Inpatient Immobility-Associated Outcomes: A Retrospective Cohort Study
Advances in Geriatric Medicine and Research
DOI: https://doi.org/10.20900/agmr20260005

Feasibility of in-bed exercise testing using a clamp-on pedaling device: A single-center pragmatic study
Global Cardiology Science & Practice
https://globalcardiologyscienceandpractice.com/index.php/gcsp/article/view/952

How can I bring Spark™ to my facility?

Join the waitlist on our website. You can also reach out directly to hello@kinetitec.com to discuss pilot programs or research partnerships.

Can Spark™ be used for research studies?

Yes. Spark's cloud-connected data capture is well-suited for research. The system provides objective, timestamped activity data that can support study endpoints related to in-bed mobility.

Still have questions?

We're here to help. Reach out directly or request a demo.