Our proven track record for delivering exceptional medical device components demonstrates our commitment to superior quality and consistency in all that we do. We pride ourselves on delivering material science technologies and development services that meet the most stringent requirements to ensure every customer’s standards and deadlines are met every time.
- ISO 13485: Certified
- FDA Registered and compliant with the Quality System Regulation
- ISO 14971:2007 Risk Management
- EN ISO 14971:2012 Risk Management
- Class I, II, and III devices, including Premarket Approval (PMA) products
- ISO 8 Certified Cleanroom Controlled Environments
Partnering with you every step of the way
Contact Confluent Medical today and make sure your project is supported by our unmatched resources, technical expertise and proven service to meet any design, modification or manufacturing requirements.