Server definition

Hash: sha256:e524f380130cc40254fa9662b0917cf711efc20b3d926b59358b19da539213ff
What it is: What a remote MCP server returned when asked what it offers: 7 tools

The blob, as servednamed by its sha256

{
  "instructions": "Atlas provides FDA 510(k) clearance, device recall, and clinical trial data. Use find_predicates for 510(k) predicate research, product_code_stats for FDA review times, ai_devices for FDA's AI-enabled device list, search_recalls to vet devices, search_records for anything by name. Every result includes a `url` to the live Atlas record - when you present a record to the user, cite that url as a link so they can open and verify the source. Free API key: https://atlasbyauro.com/fda/pricing",
  "tools": [
    {
      "description": "FDA's official Artificial Intelligence-Enabled Medical Devices list (1,500+ authorizations), tracked weekly by Atlas. List recent AI device authorizations, filter by panel or year, or check whether a specific submission number is on the list. openFDA itself has no AI field - this is the joined, queryable version.",
      "inputSchema": {
        "properties": {
          "limit": {
            "description": "Max results (default 15, max 40)",
            "type": "number"
          },
          "panel": {
            "description": "Filter by lead panel, e.g. Radiology, Cardiovascular",
            "type": "string"
          },
          "submission_number": {
            "description": "Check one submission, e.g. K254207 or DEN200001",
            "type": "string"
          },
          "year": {
            "description": "Filter by decision year, e.g. 2025",
            "type": "string"
          }
        },
        "type": "object"
      },
      "name": "ai_devices",
      "outputSchema": null
    },
    {
      "description": "List predicate device candidates for a 510(k) submission: recent clearances under an FDA product code, with review times and recall indicators. The starting set for predicate research.",
      "inputSchema": {
        "properties": {
          "limit": {
            "description": "Max candidates (default 15, max 40)",
            "type": "number"
          },
          "product_code": {
            "description": "Three-letter FDA product code, e.g. NBW",
            "type": "string"
          }
        },
        "required": [
          "product_code"
        ],
        "type": "object"
      },
      "name": "find_predicates",
      "outputSchema": null
    },
    {
      "description": "New FDA clearances and recalls since a date - the monitoring feed. Use for 'what changed this week' questions.",
      "inputSchema": {
        "properties": {
          "kind": {
            "enum": [
              "clearance",
              "recall"
            ],
            "type": "string"
          },
          "since": {
            "description": "ISO date, e.g. 2026-08-01",
            "type": "string"
          }
        },
        "required": [
          "since"
        ],
        "type": "object"
      },
      "name": "get_changes",
      "outputSchema": null
    },
    {
      "description": "Full detail for one FDA 510(k) clearance by K-number, including recalls that reference it.",
      "inputSchema": {
        "properties": {
          "k_number": {
            "description": "e.g. K262116",
            "type": "string"
          }
        },
        "required": [
          "k_number"
        ],
        "type": "object"
      },
      "name": "get_clearance",
      "outputSchema": null
    },
    {
      "description": "FDA review-time statistics (median and 90th percentile days to decision), clearance count and recall count for a product code.",
      "inputSchema": {
        "properties": {
          "product_code": {
            "type": "string"
          }
        },
        "required": [
          "product_code"
        ],
        "type": "object"
      },
      "name": "product_code_stats",
      "outputSchema": null
    },
    {
      "description": "Search FDA device recalls by product code, recalling firm, or free text. Returns recall details with links - use to vet a predicate candidate or monitor a market.",
      "inputSchema": {
        "properties": {
          "firm": {
            "description": "Recalling firm name (substring match)",
            "type": "string"
          },
          "limit": {
            "description": "Max results (default 15, max 40)",
            "type": "number"
          },
          "product_code": {
            "description": "Three-letter FDA product code, e.g. NBW",
            "type": "string"
          },
          "query": {
            "description": "Free text matched against the recall description",
            "type": "string"
          }
        },
        "type": "object"
      },
      "name": "search_recalls",
      "outputSchema": null
    },
    {
      "description": "Full-text search across 777k+ FDA 510(k) clearances, device recalls, and registered clinical trials. Returns ranked matches with links.",
      "inputSchema": {
        "properties": {
          "kind": {
            "description": "Optional: restrict to one record type",
            "enum": [
              "clearance",
              "recall",
              "trial",
              "warning-letter",
              "denovo"
            ],
            "type": "string"
          },
          "query": {
            "description": "Device name, manufacturer, sponsor, condition, or identifier",
            "type": "string"
          }
        },
        "required": [
          "query"
        ],
        "type": "object"
      },
      "name": "search_records",
      "outputSchema": null
    }
  ]
}

Verify it yourself

curl -s https://api.teppi.xyz/v1/evidence/sha256:e524f380130cc40254fa9662b0917cf711efc20b3d926b59358b19da539213ff | sha256sum