INDIVIDUAL MCP TOOL
device_postmarket_lookup
Post-clearance intelligence for one AI/ML device by 510(k) number: its product code's recalls, MAUDE adverse-event level and trend, warning-letter and 483 matches for the applicant, plus per-device drift signals (adverse-event inflection, re-clearances of the same device line, software-recall patterns, predicate-cohort recall activity).
LIVE ENDPOINT
https://constat.dev/api/mcp
Connect to this endpoint to inspect the live schema for device_postmarket_lookup and invoke it with your own arguments.
Indexed input schema
{}Risk classification
Potential side effects detected · medium confidence · heuristic, not a guarantee.
- A tool name or description contains a write-action term.
Parent server
CONNECT WITH APPROVAL
Client installation
Review this server and its permissions before adding it. Secret placeholders must be set locally.
Codex
~/.codex/config.toml
[mcp_servers.com-healthai-radar]
url = "https://constat.dev/api/mcp"
enabled = true
Claude Code
.mcp.json
{
"mcpServers": {
"com-healthai-radar": {
"type": "http",
"url": "https://constat.dev/api/mcp"
}
}
}
Claude Desktop
Settings → Connectors → Add custom connector
Name: com-healthai-radar
Remote MCP URL: https://constat.dev/api/mcp
Add this remote URL as a custom connector in Claude Desktop. Availability depends on the user plan and workspace policy.
Cursor
.cursor/mcp.json
{
"mcpServers": {
"com-healthai-radar": {
"url": "https://constat.dev/api/mcp"
}
}
}
Visual Studio Code
.vscode/mcp.json
Add to Visual Studio Code{
"servers": {
"com-healthai-radar": {
"type": "http",
"url": "https://constat.dev/api/mcp"
}
}
}
Generic MCP
Client-specific MCP configuration
{
"name": "com-healthai-radar",
"transport": "streamable-http",
"url": "https://constat.dev/api/mcp"
}
MCP Inspector
Run the official MCP Inspector locally and enter the indexed Streamable HTTP endpoint.
Related tools
device_risk_lookup— Review a medical-device category's public FDA signals by three-letter product code (e.g.firm_compliance_history— Build a recent, source-bounded FDA public-record timeline for a device firm: matched recalls, warning letters, and Form 483 citations where exact FEI numbers are available.watchlist_diff— Return machine-generated FDA public-record changes detected for monitored product codes since a caller-supplied date, plus each code's latest category snapshot and postmarket coverage.device_evidence_lookup— Look up the structured premarket evidence FDA accepted for a specific AI/ML-enabled device by 510(k) number (e.g.evidence_search— Find AI/ML device clearances by filter — product code, panel, applicant, and whether the submission reported clinical data, any sensitivity metric, or a PCCP.predicate_chain— Trace the predicate ancestry of a 510(k) device, with each cited predicate's age (how many years old the predicate was when the child cleared).evidence_cohort_stats— Reporting-rate stats across the parsed AI/ML corpus (optionally by panel).postmarket_search— Find AI/ML devices by postmarket criteria — product code, panel, applicant, whether any drift signal exists, minimum recalls in 24 months, or a rising MAUDE trend.