Gastrointestinal Endoscopy Devices – Market Insights – United States

The US GI endoscopy device market is projected to experience modest expansion through 2034. The market growth is being driven by supportive treatment and screening guidelines, the growing use of AI in GI videoscope systems, and the development and adoption of single-use duodenoscopes, all of which are expected to boost procedure volumes across the country. However, despite these positive trends, the market’s overall growth may be constrained by declining average selling prices driven by price-based competition and limited product innovation in certain segments.

This Medtech 360 Report provides comprehensive data and analysis on the state of the market for GI endoscopy devices in the US from 2019 to 2034.

Favorable CRC screening guidelines, in addition to availability of alternative screening tests will support colonoscopy procedure volumes.

How do the latest CRC screening guidelines and insurance coverage impact the overall procedure volumes?

To what extent will colonoscopy procedure volumes be impacted by alternative CRC tests?

Device innovation, along with the increasing integration of AI in GI videoscope systems will support overall growth in the GI endoscopy market.

How is the growing integration of AI impacting screening and procedure volumes?

What other device innovations are emerging in this market, and how are they expected to impact its growth?

How will AI integration affect the competitiveness of certain companies?

Major players in the GI endoscopy device market are focusing more on technological advancements, but some segments remain stagnant in terms of innovation.

How will mergers and acquisitions change the competitive landscape of the GI videoscope systems market?

Which companies are investing in AI and CAD? How is the incorporation of AI and CAD into endoscopy impacting the GI endoscopy device market?

Which companies are offering disposable duodenoscopes that are seeing a favorable adoption in the US markets? How does regulatory efforts support the adoption of single-use duodenoscopes?