For regulatory affairs & competitive intelligence teams
New 510(k) clearances in your therapeutic area.
Every new FDA 510(k) clearance — applicant, device, product code, decision date — filtered to your specialty and delivered the day it posts. Track competitors without a six-figure enterprise contract.
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Your specialty only
One therapeutic area — cardio, ortho, neuro, IVD — not the entire device market. No noise, just your field.
Inbox-ready, not raw API
No openFDA queries, no spreadsheets to clean. A clear alert the day a clearance posts — applicant, device, K-number.
Self-serve, not six figures
Sign up and pay by card — no sales call, no enterprise contract. A fraction of what the big platforms charge.
Track every new clearance in your area — the day it posts.
Get early accessBuilt from public FDA 510(k) clearance data — structured public records for informational purposes only, not regulatory advice.