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OUR JOURNEY

RIM Medical Technologies is an orthopedic and spine fusion device manufacturer. Grounded in clinical insight, we are committed to developing efficient orthopedic spine surgical devices designed to support surgeons and seamlessly integrate into existing workflow.

COMPANY HIGHLIGHTS

- 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 medical doctor with more than twenty years of clinical experience, RIM Medical Technologies is a medical device development and manufacturing company with offices in Spokane, Washington, USA, and Calgary, Alberta, Canada. Bringing ideas directly from the OR, we develop and manufacture orthopedic spine surgical devices designed to integrate seamlessly into existing workflows and improve procedural efficiency.

RIM Medical Technologies is registered with the FDA and compliant with Good Manufacturing Practices as outlined in the Quality Management System Regulation (QMSR – 21 CFR Part 820).

Our deep understanding of the specific requirements of surgical procedures—combined with close collaboration with orthopedic spine surgeons—results in thoughtfully engineered tools aligned with procedural needs.

We manufacture our devices in ISO 13485:2016–certified facilities using USP Class VI–verified materials.

Consistent quality and reliability are ensured through adherence to US FDA regulatory requirements, a Quality Management System based on the objectives of ISO 13485:2016, and rigorous auditing of trusted and verified supply chain partners.

With RIM Medical Technologies, you always have direct, comprehensive support, timely follow‑ups, less‑than‑24‑hour callbacks, and in‑person contact with the licensed medical doctor, CEO, or COO.

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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