{
  "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": "2026-09-07",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 4
    }
  },
  "results": [
    {
      "proprietary_name": [
        "TYVEK Pouch/Roll with STERRAD Chemical Indicator"
      ],
      "establishment_type": [
        "Manufacture Medical Device",
        "Manufacture Medical Device for Another Party (Contract Manufacturer)"
      ],
      "registration": {
        "registration_number": "1418005",
        "fei_number": "3003243311",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2026",
        "name": "AMCOR FLEXIBLES, LLC",
        "address_line_1": "1919 S Butterfield Rd",
        "address_line_2": "",
        "city": "MUNDELEIN",
        "state_code": "IL",
        "iso_country_code": "US",
        "zip_code": "60060",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "Amcor Flexibles",
          "owner_operator_number": "9059465",
          "official_correspondent": {
            "first_name": "Brian",
            "middle_initial": "-",
            "last_name": "Foley",
            "subaccount_company_name": "",
            "phone_number": "x-847-5736792-x"
          },
          "contact_address": {
            "address_1": "1919 South Butterfield Rd.",
            "address_2": "",
            "city": "Mundelein",
            "state_code": "IL",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "60060"
          }
        }
      },
      "pma_number": "",
      "k_number": "K103210",
      "products": [
        {
          "product_code": "FRG",
          "created_date": "2013-02-07",
          "owner_operator_number": "9059465",
          "exempt": "",
          "openfda": {
            "device_name": "Wrap, Sterilization",
            "medical_specialty_description": "General Hospital",
            "regulation_number": "880.6850",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}