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.
前公告機構首席審核員，在 EU MDR/IVDR 實施和 III 類器材 CE 認證方面擁有 15 年以上經驗。
EU MDR · IVDR · ISO 13485 · Clinical Evaluation
NMPA（中國）和 PMDA（日本）註冊路徑專家。擅長跨國監管協調和臨床試驗豁免。
NMPA · PMDA · CDSCO · TGA
專注於 FDA 510(k) 提交、De Novo 路徑和質量體系法規 (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.