AGENDA Information of Event Schedule

Focusing on the design, development, and manufacture of orthopedic devices, instruments, and implants coupled with a keen awareness of challenges associated with the space, the ODT Forum presents a comprehensive agenda that addresses many of today's more important issues.

7:00-8:40 a.m.

Registration & Continental Breakfast

Sponsored by:

8:40-8:45 a.m.

Opening Remarks

Howard Revitch, ODT Group Publisher, and Sean Fenske, ODT Editor-in-Chief

8:45-9:00 a.m.

Welcome to Memphis

An introduction of the region serving as the host of the 2026 ODT Forum—Memphis, Tenn.—and an overview of why the area is so important to the orthopedic device manufacturing industry.

speaker-1

Vernon Hartdegen

9:00-9:45 a.m.

State of the Industry

This session will provide a comprehensive overview of the happenings within the orthopedic device manufacturing industry. Supply chain, M&A, and other related topics critical to both OEMs and their supply partners will be covered.

speaker-1

David Sheppard

9:45-10:30 a.m

The ASC Disruption: Clinical and Technology Perspectives

The continued growth of ASCs and the increased number of procedures being performed within the environment have resulted in the need for innovative solutions from orthopedic device makers. This session will offer insights from both an OEM representative and a surgeon to discuss challenges, opportunities, trends, and the future vision for orthopedic procedures taking place in ASCs and the device technology to facilitate them.

Moderated by Tony Freeman

speaker-1

Melanie Prevost

speaker-2

Dr. Patrick Toy

speaker-3

Anthony S. Freeman

10:30-11:15 a.m.

Networking Break

Sponsored by:

11:15 a.m.-12:15 p.m.

Osseointegration in Modern Orthopedics

Osseointegration is a foundational biological principle in modern orthopedics, describing the direct structural and functional connection between living bone and the surface of a load-bearing implant. This panel discussion will examine the evolution of osseointegration across orthopedic applications, highlighting how advances in implant design, surface technologies, and manufacturing have improved fixation, longevity, and clinical outcomes. The session will also explore emerging technologies that may further enhance bone integration and expand the role of osseointegrated implants in orthopedics. By bringing together perspectives from surgeons, engineers, and industry leaders, the discussion aims to provide insight into both the historical development and the future direction of osseointegration-based orthopedic solutions.

Moderated by Brian McLaughlin

speaker-1

Trey Rodgers

speaker-2

Mark Morrison

speaker-3

Chuck Hansford

speaker-4

Cowan Moore

speaker-5

Brian R. McLaughlin

12:15-1:45 p.m.

Networking Luncheon

Sponsored by:

1:45-2:45 p.m.

Beyond the Backlog: Building Resilient Orthopedic Supply Chains

There are important strategies with which orthopedic OEMs and contract manufacturers can move from reactive to proactive supply chain strategies. This session will highlight lessons learned from pandemic-era disruptions and how to build resilience through several methods—regionalization and nearshoring, dual/multi-sourcing strategies, inventory segmentation and risk-based planning, and supplier collaboration and visibility tools.

Moderated by Matt Stekier

speaker-1

Juan Mangual

speaker-2

Michael Labadie

speaker-3

Matt Stekier

2:45-3:30 p.m.

A New Era for Regulatory & QMS Requirements: An FDA & EU MDR Update

While revisions are consistently taking place across all regulatory areas, it seems recent changes have been even more impactful for medical device manufacturers. Whether the dramatic change from MDD to MDR in Europe, the FDA’s implementation of QMSR, incorporation and shifting guidance related to artificial intelligence, or an enhanced focus on testing, updated regulations, and guidance documents will have a significant impact on device makers. This session will provide a high-level overview of these changes and what they mean for the management teams in the medtech industry. Avoiding “the weeds” of regulatory minutia, attendees will find out what’s important to them and why it matters for their business.

speaker-1

Christine Scifert

speaker-2

Dawn Norman, MS

3:30-4:15 p.m.

Networking Break

Sponsored by:

4:15-5:15 p.m.

The Make vs. Buy Question: Factors for the Decision

What goes into the decision to make versus buy? Is the answer always black and white or clear-cut? What factors and considerations must be used in the evaluation? Is there a middle ground or hybrid approach that can be leveraged? This session will feature a panel discussion among industry representatives who have had to address this question. They will share the best practices they use and their own recommendations for an effective evaluation.

Moderated by Monica Burt

speaker-1

Paul Vasta, Ph.D.

speaker-2

Patrick G. Fisher

speaker-3

Monica Burt

speaker-4

Janelle Swanson

speaker-5

Tim Turner

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