{"server":{"$schema":"https://static.modelcontextprotocol.io/schemas/2025-09-29/server.schema.json","_meta":{"io.mcpregistry/tags":[],"io.mcpregistry/tools":[],"io.mcpregistry/transport":"streamable-http"},"description":"FDA and CMS evidence for AI medical devices: 510(k), postmarket, reimbursement, and compliance.","name":"com.healthai/radar","remotes":[{"type":"streamable-http","url":"https://constat.dev/api/mcp"}],"repository":{"source":"github","url":"https://github.com/healthai-hq/fda-risk-radar"},"title":"Constat MCP — FDA Device Evidence Lifecycle","version":"0.5.3","websiteUrl":"https://constat.dev/connect"},"_meta":{"io.mcpregistry/official":{"status":"active","origin":"official","updated_at":"2026-09-15T03:57:33Z","synced_at":"2026-09-22T03:57:44.503431Z","is_latest":true,"published_at":"2026-09-15T03:57:33Z"}}}