• Who We Are

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    Medical Device Consultants

    From concept to commercialization.

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    FDA Regulatory & Intellectual Property Experts

    Navigate. Protect. Succeed.

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    Laser Specialists

    Proven. Performance.

  • CyMeda, Inc. specializes in the design, development, manufacture, commercialization, and service of medical lasers and devices for dermatology, cardiovascular, vascular, and ophthalmic systems.

    • Experts in 308 nm excimers, ND:YAG, CTH:YAG, Er:YAG, Q-switching, femtosecond lasers, fiber optics, and catheters

    • 5000 ft2 headquarters in Carlsbad, CA, in North County San Diego, a world-renowned hub of medical device and life sciences

    Established in 2020

    We have the talent, resources, and passion to bring innovative and life-changing medical devices to market.

  • What We Do

    Product Development

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    Medical Device Design

    Lasers • Masers • Electro-optics

    Pulse power • Software engineering

    Catheters • Semiconductors

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    Prototypes

    From initial concept to functional proof-of-concept

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    Turnkey Manufacturing

    Scalable from 1st article through commercialization

  • Regulatory and Quality Systems

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    Regulatory

    FDA 510(k) clearances • KFDA (Korea)

    NMPA (China) • CE (EU) mark

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    Quality Systems

    FDA • State of California

    Notified bodies for ISO 13485 and CE mark

  • Pharos Excimer Lasers

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    Laser Sales

    New in-box from the original manufacturer at ~50% the price of comparable lasers

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    Technical Service

    Nationwide service by the original Pharos service team

  • Strategic Services

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    Intellectual Property

    Patents • Copyrights • Trademarks

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    Commercialization

    Market segmentation • Brand creation

    Go-to-market strategy • Distribution

    B2B & B2C communications

  • Where and How We Bring Your Vision to Life

    5000 ft2 Research & Development and Manufacturing facility with state-of the-art equipment for device design, prototyping, 1st article production, and small-scale manufacturing ideal for clinical trials, regulatory clearances, quality systems creation, and market-entry.