{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-08-03",
    "results": {
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        "N22 COCHLEAR IMPLANT SYS FOR PED"
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        "Manufacture Medical Device"
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        "name": "COCHLEAR LTD.",
        "address_line_1": "14 MARS ROAD",
        "address_line_2": "",
        "city": "LANE COVE New South Wales",
        "state_code": "",
        "iso_country_code": "AU",
        "zip_code": "",
        "postal_code": "2066",
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          "name": "Laura Blair",
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          "bus_phone_num": "5235798",
          "bus_phone_extn": "",
          "fax_area_code": "",
          "fax_num": "",
          "email_address": "lblair@cochlear.com",
          "address_line_1": "10350 Park Meadows Drive",
          "address_line_2": "",
          "city": "Lone Tree",
          "state_code": "CO",
          "iso_country_code": "US",
          "zip_code": "80124",
          "postal_code": ""
        },
        "owner_operator": {
          "firm_name": "COCHLEAR AMERICAS",
          "owner_operator_number": "9076254",
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          "openfda": {
            "device_name": "Implant, Cochlear",
            "medical_specialty_description": "Unknown",
            "regulation_number": "",
            "device_class": "3"
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}