Enercon highlights end-to-end electronics capabilities for FDA-regulated medical devices

The company’s integrated approach helps customers navigate regulatory requirements, reduce development risk, and accelerate time to market.

A person looking through a microscope

CREDIT: ENERCON

Enercon, a fully integrated design, development, and manufacturing company, is exhibiting at MD&M West at the Anaheim Convention Center from February 3 to 5, at Booth 1446. The company will highlight its end-to-end electronics capabilities for FDA-regulated medical devices.

Based in the United States, Enercon supports medical device companies throughout the product lifecycle, from design and development through scalable manufacturing. Its integrated approach brings engineering and manufacturing teams together early, helping customers navigate regulatory requirements, reduce development risk, and accelerate their time to market.

“As Enercon returns to MD&M West this week, we’re looking forward to connecting with teams navigating today’s medical device development challenges,” says Brett Mancini, VP of sales and marketing at Enercon. “Our focus is on helping partners avoid common manufacturing pitfalls by balancing speed and precision through stronger cross-discipline collaboration.”

At MD&M West, Enercon will share how its Design + Build model supports early collaboration, disciplined execution, and smoother transitions from development into production. The company works with both emerging and established medical device teams to address customer-specific needs while maintaining the rigor required in regulated environments.

Whether exploring new product development or seeking a trusted electronics partner, Enercon looks forward to collaborating with medical device innovators at MD&M West.