{
  "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": "2026-10-26",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 2
    }
  },
  "results": [
    {
      "proprietary_name": [
        "Injection Kit"
      ],
      "establishment_type": [
        "Complaint File Establishment per 21 CFR 820.198",
        "Develop Specifications But Do Not Manufacture At This Facility"
      ],
      "registration": {
        "registration_number": "3013633270",
        "fei_number": "3013633270",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2027",
        "name": "ALTAVIZ, LLC",
        "address_line_1": "13766 Alton Parkway",
        "address_line_2": "Suite 143",
        "city": "Irvine",
        "state_code": "CA",
        "iso_country_code": "US",
        "zip_code": "92618",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "Altaviz, LLC",
          "owner_operator_number": "10086745",
          "official_correspondent": {
            "first_name": "Gary",
            "middle_initial": "",
            "last_name": "Holland",
            "subaccount_company_name": "",
            "phone_number": "1-303-9158013-x"
          },
          "contact_address": {
            "address_1": "13766 Alton Parkway",
            "address_2": "Suite 143",
            "city": "Irvine",
            "state_code": "CA",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "92618"
          }
        }
      },
      "pma_number": "",
      "k_number": "K231261",
      "products": [
        {
          "product_code": "GAA",
          "created_date": "2023-09-14",
          "owner_operator_number": "10086745",
          "exempt": "",
          "openfda": {
            "device_name": "Needle, Aspiration And Injection, Disposable",
            "medical_specialty_description": "General, Plastic Surgery",
            "regulation_number": "878.4800",
            "device_class": "1"
          }
        },
        {
          "product_code": "FMI",
          "created_date": "2023-09-14",
          "owner_operator_number": "10086745",
          "exempt": "",
          "openfda": {
            "device_name": "Needle, Hypodermic, Single Lumen",
            "medical_specialty_description": "General Hospital",
            "regulation_number": "880.5570",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}