MCPLow riskUnclaimed
Constat MCP — FDA Device Evidence Lifecycle
FDA and CMS evidence for AI medical devices: 510(k), postmarket, reimbursement, and compliance.
healthai.comhealthai.com/radar
server.json
{
"$schema": "https://static.modelcontextprotocol.io/schemas/2025-12-11/server.schema.json",
"name": "com.healthai/radar",
"description": "FDA and CMS evidence for AI medical devices: 510(k), postmarket, reimbursement, and compliance.",
"title": "Constat MCP — FDA Device Evidence Lifecycle",
"repository": {
"url": "https://github.com/healthai-hq/fda-risk-radar",
"source": "github"
},
"version": "0.5.3",
"websiteUrl": "https://constat.dev/connect",
"remotes": [
{
"type": "streamable-http",
"url": "https://constat.dev/api/mcp"
}
]
}Permissions
DeclaredDetected
Runs code—None
Installs—None
Runs install scripts—None
Network
constat.devconstat.devNeeds credentialsNoneNone
Outside the workspace—None
Agent tools—None
Checks
Low risk · Nothing worth a warning was found.
Not reviewed by a person · Checked by rules; the model review is not switched on yet.
Versions
- #10.5.3latestOct 7, 2026
Constat MCP — FDA Device Evidence LifecycleOpen in Codeg