Le catalogue réel des outils pour IA

FDA and CMS evidence for AI medical devices: 510(k), postmarket, reimbursement, and compliance.

FDA medical-device regulatory intelligence from keyless openFDA datasets.

Resolve a federal award and buy bounded USAspending contract lifecycle and end-date evidence.

Remplir un constat amiable et recevoir le PDF signé par email, directement en conversation.

FDA drug approvals, 510(k) device clearances, recalls and adverse-event reports.

FDA recalls: food, drugs, devices; safety alerts. Register in-session — free testnet funds.

EOL dates, risk scores, CISA KEV exposure, SBOM audits and edge-device EOS for 500+ products.

FDA AI/ML Software as a Medical Device Action Plan + 510(k) + PMA + De Novo pathways for US MedT...

Check whether an LLM model id is deprecated, retiring, or retired, and what to migrate to.

Clean FDA regulatory data: company resolution, facilities, recalls, inspections, approvals.

FDA MCP — US Food and Drug Administration public API (free, no auth)

FDA Regulations MCP — US Food & Drug Administration regulations (21 CFR).

Veterinary FDA MCP — openFDA Animal & Veterinary adverse events, pet/animal

Orange Book competitive intelligence from FDA's monthly official data ZIP.

FDA inspection outcomes, Form 483 observations, compliance actions and import refusals for drug…

Search FDA safety data: drug adverse events, recalls, and device events.

Korean listed medical AI, biotech and device companies linked to MFDS and FDA regulatory records.

Query FDA data on drugs, food, devices, and recalls via openFDA. STDIO or Streamable HTTP.

Is a foreign supplier on an FDA import alert red list, detained at the US border? 14,000+ listings.

Cross-vendor AI model lifecycle: status, sunset dates, and migration targets, source-cited.