openFDA · Example Payload

Device Classification

FDAFood and Drug AdministrationDrug SafetyAdverse EventsDrug LabelsRecallsMedical DevicesFood SafetyTobaccoPublic HealthOpen DataGovernmentRegulatoryFAERSSPL

Device Classification is an example object payload from openFDA, with 2 top-level fields. It illustrates the shape of data this provider's APIs accept or return.

Top-level fields

metaresults

Example Payload

device-classification.json Raw ↑
{
  "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": "2026-06-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 7068
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Eligible",
      "product_code": "HOA",
      "openfda": {
        "registration_number": [
          "1932180",
          "8040278",
          "9614093",
          "3008808049",
          "9615857",
          "1313525"
        ],
        "fei_number": [
          "1000119305",
          "3004216008",
          "3002802903",
          "3002409980",
          "3008808049",
          "1317628"
        ]
      },
      "review_panel": "OP",
      "medical_specialty": "OP",
      "device_name": "Compressor, Orbital",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Ophthalmic",
      "device_class": "1",
      "definition": "",
      "regulation_number": "886.4350",
      "implant_flag": "N",
      "submission_type_id": "4"
    }
  ]
}