Regulatory intelligence for teams who cannot check 27 websites every morning
MedFlux is a market intelligence terminal for medical device professionals. We aggregate safety alerts, regulatory changes, and market signals across 27 authorities and deliver them in under 90 seconds — with free tools, deep educational content, and transparent editorial standards.
WHO WE SERVE
Regulatory affairs, quality, post-market surveillance, and market access teams at device manufacturers, suppliers, and consultants. If your job depends on catching an FDA recall, NMPA update, or EU MDR change before it becomes a crisis, MedFlux is built for you.
WHAT WE BELIEVE
- People-first content over doorway pages — we prune thin programmatic URLs rather than inflate sitemaps.
- Primary sources — FDA, EUR-Lex, PMDA, NMPA and other official references are cited on deep pages.
- Free forever utility — recall lookup, 510(k) predicate finder, and Japan pathfinder stay free because they create real workflow value.
EDITORIAL BOARD
Named editorial personas review regulatory explainers and glossary depth. Bios describe domain expertise used to shape content. For standards on sourcing and corrections, see our editorial policy.
前公告机构首席审核员，在 EU MDR/IVDR 实施和 III 类器械 CE 认证方面拥有 15 年以上经验。
EU MDR · IVDR · ISO 13485 · Clinical Evaluation
NMPA（中国）和 PMDA（日本）注册路径专家。擅长跨国监管协调和临床试验豁免。
NMPA · PMDA · CDSCO · TGA
专注于 FDA 510(k) 提交、De Novo 路径和质量体系法规 (21 CFR 820) 整改。
FDA · 510(k) · PMA · 21 CFR 820
COMPANY
MedFlux is a product of Adventurer Limited. Product application: app.medflux.live. Demo: book a walkthrough.