1
Build your watchlist
Add three-letter FDA product codes and internal client labels. The public preview starts with one code.
From public records to usable intelligence in three steps
This is self-service software, not a report-writing service. Build a watchlist, run a scan and export the findings yourself.
2
Scan openFDA live
Organize clearance counts, applicants, countries, submission routes and actual review times.
3
Export a usable report
Download CSV or printable HTML output. Invited testers can evaluate broader workflows.
One workspace across multiple client product categories
Review each code separately or export them together. Every result retains a link to the underlying FDA record for professional verification.
- Adjustable 6, 12, 24 or 36-month windows
- Applicant and Taiwan-origin statistics
- Traditional, Special and third-party review mix
- Median days from receipt to clearance
- CSV and printable HTML exports
- Browser-local watchlists; no client list upload
3Product codes
87Clearances
114 daysMedian review
GEI · Electrosurgical53 records
LPL · Contact Lens18 records
DQY · Monitor16 records
Why the FDA search page alone is not enough
ClearanceRadar does not replace professional judgment. It turns repeated data-organizing work into a repeatable workflow.
3–36 mo.Adjustable monitoring window
1,000Up to 1,000 clearance records per code and scan
1 clickReturn to the FDA source for every result
EARLY ACCESS
ClearanceRadar is in small-scale testing
We are inviting a small number of medical-device regulatory consultants and regulatory teams to test the product in real workflows. Tell us about your work; when there is a fit, we will contact you at your work email to discuss testing and possible collaboration.
- Free to apply; no payment details
- Applying does not guarantee access
- No public pricing during this research stage
- No client names or confidential files required
Frequently asked questions
The product, data and testing process in plain terms.
Is this consulting or a done-for-you report service?
No. ClearanceRadar is self-service software. Users configure product codes, run searches and export reports themselves. We do not provide medical, legal, submission or regulatory consulting services.
Where does the data come from?
The workspace queries the FDA openFDA 510(k) dataset live. The FDA notes that openFDA data has not been validated, so every result retains a source link and important decisions should be checked against official FDA records.
Can I buy or subscribe today?
Not yet. ClearanceRadar is in a small closed test with no public price or online payment. Apply first; we assess fit manually and follow up by email.
Does applying guarantee access?
No. We are limiting the number of concurrent testers so we can support each participant and learn from relevant regulatory workflows.
Will my client list be uploaded?
No. Product codes, labels and report recipients stay in your browser. The application form does not ask for client names or file uploads.
Want to test your own workflow?
Share the minimum business context we need, and we will personally review your application.
Important: ClearanceRadar is data organization and monitoring software. It is not medical, legal or regulatory advice and cannot replace qualified professional judgment.