OpenFDA Regulatory Metadata vs Mdr Medical Device MCP

A side-by-side look at the OpenFDA Regulatory Metadata and Mdr Medical Device MCP MCP servers: transport, auth, tools, quality signals, and the config to install either one in Claude, Cursor, Windsurf or VS Code.

OpenFDA Regulatory Metadata logoOpenFDA Regulatory MetadataBiology & Bioinformatics · Local subprocess (stdio)Resolve FDA application numbers and product names to regulatory metadata (CDER, CBER, CDRH).56GoodAuth: not declaredMdr Medical Device MCP logoMdr Medical Device MCPBiology & Bioinformatics · Local subprocess (stdio)EU MDR (Reg 2017/745) and IVDR (Reg 2017/746) compliance for medical device + IVD manufacturers...40FairAuth: not declared

Verdict: choose OpenFDA Regulatory Metadata for biology & bioinformatics work as a local process; choose Mdr Medical Device MCP for biology & bioinformatics as a local process. You can also run both side by side in one mcpServers block.

Which MCP server should you choose?

OpenFDA Regulatory Metadata logoChoose OpenFDA Regulatory Metadata when

  • You need dedicated capabilities in the Biology & Bioinformatics domain.
  • You prefer a local stdio subprocess transport.
  • You have the keys it needs: OPENFDA_API_KEY.
  • You want tools like search_drug_label, lookup_drugsfda_application, resolve_drug_to_application.
Explore OpenFDA Regulatory Metadata

Mdr Medical Device MCP logoChoose Mdr Medical Device MCP when

  • You need dedicated capabilities in the Biology & Bioinformatics domain.
  • You prefer a local stdio subprocess transport.
Explore Mdr Medical Device MCP

Feature & specification comparison

Rows where the two servers differ are marked.

SpecOpenFDA Regulatory Metadata logoOpenFDA Regulatory MetadataMdr Medical Device MCP logoMdr Medical Device MCP
CategoryBiology & BioinformaticsBiology & Bioinformatics
Quality signal56/100 · Good40/100 · Fair
Install commandConfirmedConfirmed
TransportLocal subprocess (stdio)Local subprocess (stdio)
AuthNot declaredNot declared
PricingFreeNot declared
Required env varsOPENFDA_API_KEYNone listed
Verified ownerCommunity listingCommunity listing
GitHub stars00
Directory activity 6 views 0 installs 0 upvotes 1 views 0 installs 0 upvotes
Tools7Not listed

Tools & capabilities

OpenFDA Regulatory Metadata tools 7

  • search_drug_labelSearch openFDA drug labels (SPL) for a term.
  • lookup_drugsfda_applicationFetch Drugs@FDA application metadata for an NDA/BLA/ANDA number.
  • resolve_drug_to_applicationResolve a brand or generic drug name to its NDA/BLA application number(s). Bridges drug-name-only sources (registry inventories, product lists) to FDA regulatory metadata. Searches the brand and generic name fields directly rather than label prose, so another product merely *mentioning* this drug does not produce a false match.
  • screen_for_rwe_signalsEXPERIMENTAL. Sweep drug labels for registry / real-world-evidence signals. Searches the label corpus for terms suggesting registry, natural-history or other real-world evidence, then aggregates hits by application number with snippets showing where each term matched. **This tool is unvalidated and has a known false-positive problem.** It has no ground-truth oracle, and below the strongest hits the results are dominated by applications whose labels use "registry" in an unrelated sense. Its output is a candidate list for human review — not a finding, and not a count you should report.
  • lookup_device_submissionLook up a CDRH device submission by its number. Handles all four device pathways: 510(k) K-numbers ("K203571"), De Novo grants ("DEN160026" — stored in the 510(k) endpoint, not a separate one), PMA P-numbers ("P230044"), and HDE H-numbers. Supplement suffixes ("P230044/S001") are stripped before lookup.
  • classify_device_product_codeResolve a CDRH product code to its device class and medical specialty.
  • validate_device_applicationValidate a device number and derive class, specialty and category in one call. Chains lookup_device_submission -> classify_device_product_code, which is the full three-hop resolution: number -> product_code -> classification.

Mdr Medical Device MCP tools

No tool names declared yet. Check the project README from the listing page.

Ready-to-paste client configs

Paste either block (or both) into your client config, e.g. claude_desktop_config.json or ~/.cursor/mcp.json. We only show a config when the install command is confirmed.

OpenFDA Regulatory Metadata

mcpServers (Claude Desktop / Cursor)
{
  "mcpServers": {
    "openfda-regulatory-metadata": {
      "command": "uvx",
      "args": [
        "openfda-mcp"
      ],
      "env": {
        "OPENFDA_API_KEY": "YOUR_OPENFDA_API_KEY_HERE"
      }
    }
  }
}

Mdr Medical Device MCP

mcpServers (Claude Desktop / Cursor)
{
  "mcpServers": {
    "mdr-medical-device-mcp": {
      "command": "uvx",
      "args": [
        "mdr-medical-device-mcp"
      ]
    }
  }
}

Frequently asked questions

OpenFDA Regulatory Metadata is categorized under Biology & Bioinformatics and uses a local stdio subprocess. Mdr Medical Device MCP belongs to Biology & Bioinformatics and uses a local stdio subprocess. Pick OpenFDA Regulatory Metadata for biology & bioinformatics work and Mdr Medical Device MCP for biology & bioinformatics.

Copy the mcpServers block from the config section on this page into your client's config (for example claude_desktop_config.json or ~/.cursor/mcp.json), then fully restart the client.

OpenFDA Regulatory Metadata is listed as free. Mdr Medical Device MCP has no declared pricing — check the project's own site. If a server needs environment variables such as API keys, define them under the env key in your client's MCP config.

Yes. MCP clients support multiple servers: add openfda-regulatory-metadata and mdr-medical-device-mcp as separate keys in the same mcpServers object, and your assistant will call tools from either one.

On AllMCPs, OpenFDA Regulatory Metadata has a quality signal of 56/100 (Good) with 6 views, 0 installs and 0 GitHub stars. Mdr Medical Device MCP has 40/100 (Fair) with 1 views, 0 installs and 0 GitHub stars.