{
  "card_url": "https://itha.ai/c/medtronic.com/card.json",
  "status": "unclaimed",
  "updated_at": "2026-08-25",
  "revision": 1,
  "provenance_url": "https://itha.ai/c/medtronic.com/provenance.json",
  "card": {
    "icp": {
      "regions": [
        "global"
      ]
    },
    "itha": "0.1",
    "company": {
      "hq": {
        "city": "Galway",
        "country": "IE"
      },
      "url": "https://www.medtronic.com",
      "name": "Medtronic",
      "domain": "medtronic.com",
      "founded": 1949,
      "same_as": [
        "https://en.wikipedia.org/wiki/Medtronic",
        "https://www.wikidata.org/wiki/Q642189",
        "https://www.linkedin.com/company/medtronic"
      ],
      "employees": {
        "min": 95000
      },
      "legal_name": "Medtronic plc",
      "description": "Global healthcare technology company that designs, manufactures, and sells medical devices and therapies, including cardiac devices, surgical robotics, surgical tools, and patient monitoring systems, for more than 70 health conditions.",
      "identifiers": {
        "lei": "549300GX3ZBSQWUXY261"
      }
    },
    "offerings": [
      {
        "id": "hugo-ras",
        "url": "https://news.medtronic.com/2025-12-03-Medtronic-announces-FDA-clearance-of-Hugo-TM-robotic-assisted-surgery-system-for-urologic-surgical-procedures",
        "kind": "hardware",
        "name": "Hugo RAS System",
        "role": "manufacturer",
        "summary": "Modular robotic-assisted surgery platform. FDA-cleared in the US for urologic procedures (prostatectomy, nephrectomy, cystectomy); used in 30+ countries outside the US.",
        "certifications": [
          {
            "id": "fda_510k",
            "issuer": "U.S. Food and Drug Administration (FDA)",
            "status": "third_party_certified",
            "evidence_url": "https://news.medtronic.com/2025-12-03-Medtronic-announces-FDA-clearance-of-Hugo-TM-robotic-assisted-surgery-system-for-urologic-surgical-procedures"
          }
        ]
      },
      {
        "id": "stealth-axis",
        "url": "https://news.medtronic.com/2026-02-13-Medtronic-receives-FDA-clearance-for-Stealth-AXiS-TM-surgical-system,-first-integrated-planning,-navigation-and-robotics-platform-for-spine-surgery",
        "kind": "hardware",
        "name": "Stealth AXiS System",
        "role": "manufacturer",
        "summary": "Integrated planning, navigation, and robotics platform for spine surgery with LiveAlign real-time motion tracking. FDA-cleared for spine procedures in the US.",
        "certifications": [
          {
            "id": "fda_510k",
            "issuer": "U.S. Food and Drug Administration (FDA)",
            "status": "third_party_certified",
            "evidence_url": "https://news.medtronic.com/2026-02-13-Medtronic-receives-FDA-clearance-for-Stealth-AXiS-TM-surgical-system,-first-integrated-planning,-navigation-and-robotics-platform-for-spine-surgery"
          }
        ]
      },
      {
        "id": "affera-mapping-ablation",
        "url": "https://news.medtronic.com/2024-10-24-A-new-paradigm-in-electrophysiology-Medtronic-receives-FDA-approval-of-Affera-TM-Mapping-and-Ablation-System-and-Sphere-9-TM-Catheter",
        "kind": "hardware",
        "name": "Affera Mapping and Ablation System with Sphere-9 Catheter",
        "role": "manufacturer",
        "summary": "All-in-one high-density mapping and dual-energy (pulsed field/RF) ablation system with Sphere-9 catheter; FDA-approved for persistent AFib and atrial flutter.",
        "certifications": [
          {
            "id": "fda_pma",
            "issuer": "U.S. Food and Drug Administration (FDA)",
            "status": "third_party_certified",
            "evidence_url": "https://news.medtronic.com/2024-10-24-A-new-paradigm-in-electrophysiology-Medtronic-receives-FDA-approval-of-Affera-TM-Mapping-and-Ablation-System-and-Sphere-9-TM-Catheter"
          },
          {
            "id": "ce",
            "status": "self_declared",
            "evidence_url": "https://news.medtronic.com/2024-10-24-A-new-paradigm-in-electrophysiology-Medtronic-receives-FDA-approval-of-Affera-TM-Mapping-and-Ablation-System-and-Sphere-9-TM-Catheter"
          }
        ]
      },
      {
        "id": "micra",
        "url": "https://news.medtronic.com/2023-05-01-Medtronic-receives-FDA-approval-for-its-next-generation-Micra-leadless-pacing-systems",
        "kind": "hardware",
        "name": "Micra Leadless Pacemaker",
        "role": "manufacturer",
        "summary": "Leadless transcatheter pacemaker implanted inside the heart, less than one-tenth the size of traditional pacemakers. Median battery life up to 17 years.",
        "certifications": [
          {
            "id": "fda_pma",
            "issuer": "U.S. Food and Drug Administration (FDA)",
            "status": "third_party_certified",
            "evidence_url": "https://news.medtronic.com/2023-05-01-Medtronic-receives-FDA-approval-for-its-next-generation-Micra-leadless-pacing-systems"
          }
        ]
      },
      {
        "id": "evolut-tavr",
        "url": "https://news.medtronic.com/2025-03-30-Medtronic-Evolut-TM-TAVR-system-shows-durable-clinical-outcomes-and-outstanding-valve-performance-at-five-years-in-low-risk-aortic-stenosis-patients",
        "kind": "hardware",
        "name": "Evolut TAVR System",
        "role": "manufacturer",
        "summary": "Supra-annular, self-expanding transcatheter aortic valve replacement system for severe aortic stenosis, indicated across surgical-risk categories including low-risk."
      },
      {
        "id": "brainsense-adaptive-dbs",
        "url": "https://news.medtronic.com/2025-02-24-Medtronic-earns-U-S-FDA-approval-for-the-worlds-first-Adaptive-deep-brain-stimulation-system-for-people-with-Parkinsons",
        "kind": "hardware",
        "name": "BrainSense Adaptive DBS",
        "role": "manufacturer",
        "summary": "Closed-loop deep brain stimulation feature that self-adjusts therapy in real time to a patient's brain activity; used with Percept implantable neurostimulators for Parkinson's disease.",
        "certifications": [
          {
            "id": "fda_pma",
            "issuer": "U.S. Food and Drug Administration (FDA)",
            "status": "third_party_certified",
            "evidence_url": "https://news.medtronic.com/2025-02-24-Medtronic-earns-U-S-FDA-approval-for-the-worlds-first-Adaptive-deep-brain-stimulation-system-for-people-with-Parkinsons"
          }
        ]
      }
    ],
    "updated_at": "2026-08-25"
  }
}