Your Technical Eyes
on the Ground in Asia.
The Vorex Story
Vorex was founded by MedTech engineering veterans with over 14 years of hands-on industrial experience. We identified a critical gap in the global medical device supply chain: the disconnect between high-level R&D design requirements and actual factory-floor execution.
For Class II and III sterile medical devices, "good enough" is a regulatory risk. Compliance cannot be audited from a distance. It must be verified on-site, directly within ISO Class 7/8 cleanrooms, by experts fluent in IQ/OQ/PQ validation, precision injection molding, and terminal sterilization protocols (Gamma & ETO).
Technical Depth
We speak the language of engineers, ensuring every injection mold, assembly process, and SBS seal meets your exact CAD and DFM specifications.
Compliance First
Every manufacturing partner is strictly audited against ISO 13485:2016 and FDA 21 CFR 820, ensuring your QMS extends seamlessly into Asia.
On-site Reality
Transparency through direct presence. We provide real-time reporting and CAPA management directly from the cleanroom floor to your headquarters.