Nectar Product Development

Medical Device Start-Up Program soon to be Revealed

Long Beach, California – October 6, 2017 – Strategic partners, Nectar Product Development and Med Tech Directory, announced a new program for 2018 dedicated to helping medical device Start-Ups and Entrepreneurs launch their business.

Med Tech Council was hosted by Nectar on Monday, October 2nd, 2017, for a medical device focused networking event. Industry professionals gathered for a discussion around the future of the rapidly changing industry. The growing industry has attracted many new Start-Ups and Entrepreneurs, which Med Tech Council is designed for.

An excitement grew at the Med Tech Council event as Darren Saravis, CEO of Nectar, hinted at a new program tailored to assisting Start-Ups and Entrepreneurs in the development of medical devices. Alongside Nectar, Dan Golka, CMO of Med Tech Directory, presented the audience with a fresh take on a carefully selected group of leading medical device service providers, who will be valuable resources to the Start-Up program network. When these providers work together, it becomes a recipe for business success.

The medical device community is awaiting another year of mass expansion of device innovations. Nectar and Med Tech Directory have a wealth of experience working with various medical devices and have processes to streamline development and business needs. The strategic partners are ready to aid new companies reach their goals.

The Start-Up program will be released in January of 2018, at which time enrollment will be open to Start-Up companies. More details will be released as the development of the network proceeds.  Nectar Product Development and Med Tech Directory are excited to reveal this unique opportunity to medical device Start-Ups and Entrepreneurs.

Nectar is an award-winning design & engineering consultancy with a specialization in medical device development. We are proudly 13485 certified, we adhere to the highest industry standards. Nectar has been an industry leader in Southern California for over 25 years. Our proven user-centered design process has facilitated the successful launch of hundreds of products in the market.

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    We are an ISO 13485-certified design and engineering firm based in Southern California, specializing in the development of cutting-edge medical devices.

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