At Dravon we have a thoroughly documented Quality Management System, with a strong core of integrity. Our specifications and processes for your product are made to your requirements alongside our own. Your designs and tooling will be controlled with the same attention to detail and function as we maintain our own.

• Our trained Quality Inspectors inspect incoming components against a specification before they are approved for use in manufacture.
• The manufactured product is not released from the facility until our Quality Control Department confirms that all specifications are met.
• Our cleanrooms are ISO class 7
• Dravon is certified to ISO 13485:2016 and EN ISO 111355-2016. See the current certificate here.
• Further, Dravon is an FDA registered medical device establishment, registration #3021643.
• We are dedicated to making a medical device that performs for you and your customers exactly as it needs to, every time.

Dravon Medical Inc. Quality Policy:

Dravon has made a commitment to provide products and services of the highest quality to its customers, on time, every time. Dravon will strive to accomplish this by making each employee responsible for quality workmanship through training, recognition, and by providing the best possible working environment.