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Medical technology company
RIM Medical Technologies

RIM MEDICAL TECHNOLOGIES 
ORTHOPEDIC AND SPINE MEDICAL DEVICE MANUFACTURER

RIM Medical Technologies is a physician-led orthopedic and spine medical device manufacturer of the Rimmedtech™ Bone Dust Trap, a patented intraoperative bone graft recovery device for orthopedic and spine surgical procedures. We develop innovative medical technology designed to integrate into established surgical workflows while supporting efficient collection of locally generated autologous bone particulate during orthopedic and spine procedures.

COMPANY HIGHLIGHTS

- Physician-led medical device company

- Orthopedic & spine surgery
 

- Founded in 2018

- FDA Registration Number: 3017970304. Quality Management System Regulation (QMSR) compliance maintained

Manufacturing, packaging, and sterilization processes are validated and performed in ISO 13485:2016–certified facilities

- Class 8 cleanroom manufacturing

- Patented in Canada, United States, European Union, United Kingdom, and Japan

- Biocompatibility and performance testing completed in accordance with applicable standards

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TECHNOLOGY DEVELOPED BY MEDICAL DOCTOR

Established in 2018 by a physician with more than 20 years of clinical experience, RIM Medical Technologies is a physician-led orthopedic and spine medical device manufacturer with offices in Spokane, Washington, USA, and Calgary, Alberta, Canada. Inspired by real operating room experience, we develop innovative orthopedic and spine surgical devices designed to integrate seamlessly into established surgical workflows.

RIM Medical Technologies is registered with the U.S. Food and Drug Administration (FDA) and operates under a Quality Management System aligned with the FDA Quality Management System Regulation (QMSR – 21 CFR Part 820).

Our firsthand clinical experience, combined with close collaboration with orthopedic spine surgeons, guides the development of practical medical devices engineered to address real procedural needs while maintaining simplicity of use.

Our products are manufactured in ISO 13485:2016-certified facilities using USP Class VI–verified materials. Product quality and consistency are supported through supplier qualification, routine supplier audits, manufacturing controls, and a Quality Management System based on ISO 13485:2016 and applicable U.S. FDA regulatory requirements.

RIM Medical Technologies is committed to responsive customer support, providing direct access to company leadership—including licensed medical professionals—for technical, clinical, and product-related assistance.

The Rimmedtech™ Bone Dust Trap, reflects RIM Medical Technologies' commitment to developing practical technologies that address everyday challenges in orthopedic and spine surgery.

OUR JOURNEY SO FAR

  • 2018 - 2019

    •Incorporated in Calgary, AB, Canada

    •Design and development

    •Patent is filed with CIPO

    2020 - 2021

    •EU, USA and Japan patents filing

    •Engineering and prototyping

    •Suppliers approval

    2021 - 2022

    •EU, USA and Japan patents filing

    •Canadian patent is granted

    •Manufacturing process validation

    2023 - 2024

    • EU, USA, and Japan patents are granted

    • Packaging and sterilization processes validation

    • Device Testing

    • FDA registration

    • Manufacturing begins

    2024 - 2026

    • China patent is granted

    • FDA officially confirms Class II 510 (k) exempt

    • Initial positive feedback from surgeons received

    • Affiliated company registered in Spokane, WA, USA

    • US commercialization

    • Initiation of EU market expansion 

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