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Saylor Innovations Data Desk – FDA MAUDE Medical Device Event Reports
x402
Saylor Innovations Data Desk – FDA MAUDE Medical Device Event Reports is a paid API for AI agents from saylorinnovations.com, paid per call via x402, $0.01/call, status unknown (last checked 2026-10-17).
Returns FDA MAUDE adverse event report counts (deaths, injuries, malfunctions) plus top manufacturers and brands for any medical device type
Price / call$0.01
Success—
StatusUnknown
How this service works
Medical device event reports - FDA MAUDE malfunction, injury and death counts with top manufacturers and brands for any device type
Output
A JSON object containing the queried device name, total FDA MAUDE reports on file, raw counts and percentages for deaths, injuries, and malfunctions, an array of top manufacturers with their report counts, an array of top brands, the data source attribution, the timestamp the check was run, and an optional contextual note about interpreting the data.
Example use cases
Pre-purchase device safety research
“Before my hospital buys new infusion pumps, can you check the FDA MAUDE data on infusion pumps — how many adverse events, deaths, and injuries are on record, and which brands have the most reports?”
Journalist investigating implant safety
“I'm writing a story on hip implant safety — can you get me the FDA adverse event counts for hip prostheses, the breakdown between deaths, injuries, and malfunctions, and the top manufacturers flagged?”
Regulatory compliance device audit
“I need to benchmark our defibrillator against the industry — pull the FDA MAUDE malfunction, injury, and death totals for defibrillators and list the top manufacturers by report volume.”
Technical details
Endpoint
GEThttps://saylorinnovations.com/api/medical/device-events?utm_source=zero.xyzWhen to prefer
Choose this endpoint when you need aggregated FDA MAUDE adverse event statistics — death, injury, and malfunction counts with manufacturer breakdowns — for a specific medical device type. Prefer this over raw FDA API access when you want pre-aggregated counts and ranked manufacturer lists in a single call rather than parsing raw event records yourself.
Side effects
- Unknown or unrecognized device type returns empty or zero-count results
- Misspelled device name may not match FDA taxonomy, returning no data
- FDA MAUDE database connectivity issues may return null source or stale checked_at
- Very niche or newly classified device types may have sparse records
- Rate limiting or payment failure returns HTTP 402
Input
Schema · Request body
| Field | Type | Description |
|---|---|---|
| inputrequired | object | |
| output | object |
Tags
x402
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