Medical Device and Diagnostic Industry (MDDI)

Medical Device and Diagnostic Industry (MDDI)

MD&DI is a specialized magazine focused on the medical device and diagnostic sector, published by UBM Canon based in Los Angeles. The magazine features peer-reviewed articles that tackle various technological challenges, as well as summaries of important business, industry, and regulatory matters. Since its founding in 1979, MD&DI has evolved from a print publication, which had a monthly circulation of 48,040 in 2009, to a fully online platform boasting a claimed readership of 89,000.

National, Trade/B2B
English
Magazine

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Domain Authority
63
Ranking

Global

#504730

United States

#237861

Health/Health

#4388

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Articles

  • 2 days ago | mddionline.com | Rob Spiegel

    Superior Sensor Technology has announced the expansion of its CP Series with the introduction of the CP203 and CP303 dual pressure sensors provide new features and functionality in sleep apnea devices. These advanced sensors are the first in the series to include an integrated snore detection capability, delivering real-time data to optimize therapy and improve user experience. Launched in May 2025, the CP203 and CP303 advanced sensors build on the company's NimbleSense architecture.

  • 2 days ago | mddionline.com | Lisa McTigue Pierce |Kassandra Kania

    Personalised advertising and content, advertising and content measurement, audience research and services developmentStore and/or access information on a deviceYou can choose how your personal data is used.

  • 3 days ago | mddionline.com | Amanda Pedersen

    Trivia Tuesday: When was artificial intelligence first mentioned in MD+DI? In recognition of FDA's agency-wide AI integration for scientific reviews, this week's Trivia Tuesday question explores how far back the term "artificial intelligence" goes in MD+DI's digital archives. We were surprised to see the first mention of AI in the publication dates all the way back to March 1996.

  • 3 days ago | mddionline.com | Amanda Pedersen

    FDA plans to fully integrate the use of artificial intelligence (AI) internally across all FDA centers by the end of June, following the completion of a generative AI pilot for scientific reviewers. Yes, this means your next medical device submission to FDA will likely be reviewed, in part, by AI. “I was blown away by the success of our first AI-assisted scientific review pilot.

  • 3 days ago | mddionline.com | David Hutton

    Aptar CSP Technologies has opened a new cGMP-compliant manufacturing facility in New Jersey to produce specialized packaging solutions for pharmaceutical products, expanding its capacity to protect sensitive drugs from degradation and contamination.

Medical Device and Diagnostic Industry (MDDI) journalists

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123 Example Street

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+1 (555) 123-4567

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