industry

Medical Device Development

Since 1994, Eclipse has focused on medical device development. In fact, we were founded by a medical device design expert and plastics engineer. Our diverse team has thousands of hours of direct experience in the operating room, clinical, and point of care environments. Our staff members collectively benefit from decades of experience solving medical device, equipment, and disposable design challenges.

Areas of Expertise

Hand held surgical tools

Human Factors & Usability Testing

Turnkey regulatory support for 510(K) submission

FDA/Regulatory Compliance (Development & Evaluation)

V&V testing and evaluation

Risk analysis (FMEA, FTA, Design reviews)

Alpha prototypes device fabrication with QC

We excel at meeting usability, ergonomic, and regulatory requirements.

What class medical device do you have?

Medical devices are classified based on the risks associated with the use of the device. Devices are classified as Class I, Class II, or Class III — with Class I being the lowest risk and Class III the highest risk.

Class I – These are devices that present minimal potential for harm to the user. Examples include enema kits and elastic bandages. 35% of medical device types are Class I and 93% of these are exempt from pre-market review.
Class II –These are devices that generally present a moderate risk of harm to the user. Examples of Class II devices include powered wheelchairs and some pregnancy test kits. 53% of device types are Class II, most of which require FDA review through premarket notification (510(k)).
Class III – These are devices that sustain or support life, are implanted, or present potential high risk of illness or injury. Examples of Class III devices include implantable pacemakers and breast implants. 9% of device types are Class III and require FDA review through premarket approval (PMA) or humanitarian device exemption (HDE).
Unclassified/Not classified – These are device types that FDA has not yet classified. 3% of device types are unclassified/not classified.
Some devices may be considered “exempt”. If a device is considered “exempt”, the manufacturer would not be required to submit a premarket notification submission [510 (k) submission] and obtain FDA clearance before marketing the device in the U.S.

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