Are you a medical device developer looking for a way to bridge the gap between early product development and clinical trials? FineLine can help. We offer a material and processing combination that results in parts that pass USP Class VI testing for biocompatibility and cytotoxicity, as well as ISO 10993 Part 5 Cytotoxicity and Part 10 Irritation and Sensitization. No longer do you need to invest the time and capital into tooling up an early stage design just to make parts for clinical trials. Roll the clinical trials into the iterative process and arrive at a better finished device in the end — for less!

FineLine can process your parts in conformance to these requirements, give you a certificate of conformance with material and lot traceability, and double-bag them so that you can flow them into your sterilization process while avoiding particulates. Just choose Watershed (Biocompatible) when you upload your design for quoting, and let us do the rest.