Robert “Bob” Lundberg

Robert “Bob” Lundberg is a Regulatory/Clinical professional with a strong background in engineering and medical device development who partners with companies and regulatory authorities to introduce novel solutions that exceed company, customer and patient expectations. After spending over two decades working in Regulatory Affairs, Clinical and Quality for multibillion dollar brands and startups, Bob knows from personal experience what truly drives innovation, quality, clinical and regulatory success—and it is not mastering how to persuade people. It is how well you partner and connect with people working with you and communicate understanding back to them.

Bob has a diverse background in the medical device industry working with global ophthalmic, neurovascular, cardiovascular and other medical technology companies. He has held increasingly responsible positions from Principal Engineer to Sr. Vice President. Most recently Bob was the SVP Regulatory/Quality/Clinical at PresbiBio, LLC and Vice-President Global Regulatory Affairs, Surgical at Alcon. In these roles he has helped these organizations expand their global foot print through partnered approvals and registrations.

Bob’s ophthalmic experience includes working as a Certified Ophthalmic Technician while completing his undergraduate work, working at TOMEY Corporation, Second-Sight Medical, STAAR Surgical, Alcon, and PresbiBio, LLC.

Bob holds a Bachelor of Science degree in electrical engineering and an MBA in technology management.

Note: LSM is not yet FDA approved or available in the United States. It is currently in clinical trials only in select areas outside of the United States.

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