• BMC Medical Manufacturing
      Now ANVISA certified (Classes I-IV)
    • Cost-Efficient
      Environment
      Skilled Labor, Scalable Capacity and In-house EtO Sterilization
    • Ideally
      Located
      Monterrey, Nuevo Leon is a thriving industrial zone in Mexico directly adjacent to
      the largest medical device market in the world, the US.

    End-to-end contract manufacturing with advanced design support, scalable production technologies, and certified quality systems to bring your medical devices to market with speed and compliance.


    About us

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    Awesome Image

    With over 15 years of experience, BMC is a global contract manufacturer of high-quality medical devices, offering competitive cost advantages from an ideal business location. We assemble, package, and sterilize in-house (EtO) to maximize efficiency. Based in Monterrey, Nuevo León, a major industrial hub strategically located near the U.S. border.

    Vision

    To be the trusted contract manufacturing partner —delivering compliant, quality-assured, manufacturing-focused design solutions that de-risk programs, accelerate time-to-market, and strengthen total product economics.

    Mission

    We build long-term partnerships by combining disciplined quality, manufacturing-focused design expertise, and efficient execution—reducing risk and accelerating launch with unmatched value.

    Quality Policy

    At BMC Medical Manufacturing we are committed to designing, developing and manufacturing medical devices under a Quality Management and Continuous Improvement System, through highly qualified personnel that allows us to comply with Good Manufacturing Practices and with the requirements of our clients and the regulations that govern our industry.

    Certifications

    ISO 13485:2016


    FDA Registration as Contract Manufacturer and Contract Sterilizer 


    COFEPRIS NOM-241 Medical Devices GMP


    ANVISA GMP Medical Devices Certification (Classes I-IV)


    Quick and Efficient Technology Transfers

    This is our core model, focused to manufacture from Class I to Class III devices.

    Production Line Ramp-up

    Capacity and infrastructure ready to scale.

    Expert Support

    Engineering, quality, and production working together to ensure smooth transfers.

    Services

    Contract Manufacturing

    Delivering high-quality medical devices through scalable, ISO 13485—certified contract manufacturing processes, fully compliant with FDA, ANVISA and COFEPRIS standards.

    Research and Development

    Practical engineering for transfer, design-for- manufacturing, fixtures, and fast pilots—focused on getting your line running.

    Quality Management

    Guided by ISO 13485 standards, our Quality Management System ensures rigorous testing, regulatory compliance, and continuous improvement to guarantee the safety and reliability of every device.


    Sterilization

    In-house ETO sterilization offers a proven, reliable method to ensure the safety and sterility of medical devices.

    Validation

    Rigorous validation of equipment, processes, sterilization, and final products to ensure consistent performance and reliability at every stage.

    Medical Device Approval

    We conduct testing, prepare comprehensive documentation, and support regulatory submissions to achieve medical device approvals from global health authorities.



    Frequently Asked Questions

    Why manufacture in Mexico?

    Nearshoring in Mexico reduces costs, shortens lead times, and offers proximity to the U.S., while maintaining FDA and COFEPRIS compliance.

    Why partner with us?

    We are ISO 13485 certified, FDA registered, and COFEPRIS compliant, with validated processes and scalable production for medical devices.

    What types of devices can you manufacture?

    We specialize in endovascular and cardiovascular devices, as well as a wide range of medical device components and assemblies.

    Do you support startups and small companies?

    Yes, we help startups and emerging companies scale from prototypes to full production with tailored solutions.

    What certifications and approvals do you hold?

    ISO 13485 QMS, FDA Registration, and COFEPRIS NOM-241 GMP certification.

    How do you protect client IP?

    We sign strict NDAS and follow secure processes to protect intellectual property at every stage.

    Can I visit your facilities?

    Yes, we welcome audits and site visits by clients and regulatory authorities.

    Do you offer validation and sterilization services?

    Yes, including process validation, equipment validation, and ETO sterilization.

    What are your typical lead times?

    Lead times vary by project, but nearshoring allows us to shorten development and production cycles significantly compared to overseas manufacturing.

    How do I start a project with you?

    Contact us to schedule a meeting. We'll review your project requirements and provide a tailored proposal.

    News

    ANVISA grants GMP for Class I-IV Devices to BMC

    We have obtained ANVISA’s Good Manufacturing Practices (GMP) certification for medical devices of Classes I, II, III, and IV, covering the full spectrum of medical device risk categories.

    Elevating Mexico’s Medical Device Industry

    Leaders from health authorities and biomedical engineering institutions visited BMC

    BMC drives clinical success of catheter

    At BMC, we specialize in contract manufacturing for the medical device industry, partnering with innovators to transform early-stage concepts into market-ready solutions.

      Clients

    Our clients

    Our Team

    Alberto Peña, General Manager
     

    ALBERTO PEÑA

    General Manager

    Osmel Pérez, Operations Chief
     

    OSMEL PÉREZ

    Operations Chief

    Anna Medina, R&D Leader
     

    ANNA MEDINA

    R&D Leader

    Estrella Román, Health Manager
     

    ESTRELLA ROMÁN

    Health Manager

    Ana Lucía González, Validation Supervisor
     

    ANA LUCÍA GONZÁLEZ

    Validation Supervisor

    Mitzi Avendaño, Regulatory Affairs Responsible
     

    MITZI AVENDAÑO

    Regulatory Affairs Responsible

    Danna Salazar, Marketing Analyst
     

    DANNA SALAZAR

    Marketing Analyst

    Contact

    End-to-end contract manufacturing with advanced design support, scalable production technologies, and certified quality systems to bring your medical devices to market with speed and compliance.

    USA

    Location: 2916 N Miami Ave. Ste 621. Miami FL 33127, USA.
    Phone: +1 (786) 668 7715


    MEXICO

    Location: Blvd TLC, Parque Industrial Millenium Apodaca, N.L. Mexico.
    Phone: +52 81 8371 7614


    Mail: info@bmcmm.com
    Hours: Mon - Fri de 9:00 a 18:00 hrs. UTC-06:00