{
  "format": "devicerts.manufacturer.v1",
  "cite_as": "Lifecare, Ltd. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/lifecare-ltd (data as of 2026-11-15).",
  "source": {
    "canonical_url": "https://devicerts.com/manufacturers/lifecare-ltd",
    "json_url": "https://devicerts.com/manufacturers/lifecare-ltd.json",
    "markdown_url": "https://devicerts.com/manufacturers/lifecare-ltd.md",
    "publisher": "deviCERTS (devicerts.com)",
    "data_sources": [
      {
        "registry": "FDA 510(k)",
        "url": "https://open.fda.gov/apis/device/510k/"
      }
    ],
    "eudamed_record_synced": null,
    "fda_recalls_as_of": "2026-11-01",
    "registry_facts_computed": "2026-11-14",
    "status_as_of": "2026-11-15",
    "license": "CC BY 4.0",
    "license_url": "https://creativecommons.org/licenses/by/4.0/",
    "license_scope": "The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.",
    "attribution": "DevicErts, https://devicerts.com/manufacturers/lifecare-ltd",
    "disclaimer": "Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails."
  },
  "manufacturer": {
    "name": "Lifecare, Ltd.",
    "url": "https://devicerts.com/manufacturers/lifecare-ltd",
    "registered_as": null,
    "abbreviated_name": null,
    "also_registered_as": [],
    "country": "Israel",
    "country_basis": "FDA applicant, unverified",
    "eudamed_status": null,
    "verified": false,
    "roles": [
      "Manufacturer"
    ],
    "registrations": [],
    "identifiers": [],
    "summary": "Lifecare, Ltd. is a medical device manufacturer, with 3 devices listed in FDA 510(k) (FDA Class II) as of 15 Nov 2026.",
    "noindex": false
  },
  "counts": {
    "devices": 3,
    "devices_note": null,
    "certificates": 0,
    "fda_recalls_matched_by_name": 0,
    "fda_recalls_ongoing": 0,
    "fda_recalls_ongoing_recent": 0,
    "fda_recalls_ongoing_before": null,
    "fda_establishments": 0,
    "sites": 0
  },
  "registry_facts": {
    "covers": "Every device of the manufacturer. A device listed in two registries counts in both.",
    "registries": [
      {
        "registry": "FDA 510(k)",
        "devices": 3
      }
    ],
    "device_classes": [
      {
        "class": "FDA Class II",
        "devices": 3
      }
    ],
    "top_emdn_categories": []
  },
  "related": {
    "site_of": null,
    "part_of": null,
    "sites": [],
    "authorised_representatives": []
  },
  "devices": {
    "shown": 3,
    "total": 3,
    "all_devices_url": "https://devicerts.com/manufacturers/lifecare-ltd",
    "items": [
      {
        "name": "Lifecare Compact Tens Device",
        "url": "https://devicerts.com/devices/lifecare-compact-tens-device-gzj",
        "model_reference": "K003369",
        "device_class": "Class II",
        "registries": [
          "510(k)"
        ],
        "status": "Active",
        "decision_date": "2001-03-08",
        "open_recall": false
      },
      {
        "name": "Livia",
        "url": "https://devicerts.com/devices/livia-nuh-k163153",
        "model_reference": "K163153",
        "device_class": "Class II",
        "registries": [
          "510(k)"
        ],
        "status": "Active",
        "decision_date": "2017-06-28",
        "open_recall": false
      },
      {
        "name": "Livia",
        "url": "https://devicerts.com/devices/livia-nuh",
        "model_reference": "K183110",
        "device_class": "Class II",
        "registries": [
          "510(k)"
        ],
        "status": "Active",
        "decision_date": "2020-05-04",
        "open_recall": false
      }
    ]
  },
  "certificates": [],
  "recalls": []
}