{
  "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": "2026-08-31",
    "results": {
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Badia Polesine",
      "advisory_committee_description": "Dental",
      "address_1": "Via Cà Mignola Nuova 1699",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "POW",
      "openfda": {
        "device_name": "Crown And Bridge, Long-Term Temporary, Resin",
        "medical_specialty_description": "Dental",
        "regulation_number": "872.3770",
        "device_class": "2",
        "registration_number": [
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      "zip_code": "45021",
      "applicant": "Dental Manufacturing S.p.A.",
      "decision_date": "2026-08-05",
      "decision_code": "SESE",
      "country_code": "IT",
      "device_name": "Ruthinium Disc",
      "advisory_committee": "DE",
      "contact": "Barbara  Piazza",
      "expedited_review_flag": "",
      "k_number": "K261456",
      "state": "",
      "date_received": "2026-05-01",
      "review_advisory_committee": "DE",
      "postal_code": "45021",
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}