{
  "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": "2026-07-27",
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      "supplement_number": "S020",
      "applicant": "Prollenium Medical Technologies, Inc.",
      "street_1": "138 Industrial Pkwy. N.",
      "street_2": "",
      "city": "Aurora",
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      "zip": "L4G 4C3",
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      "advisory_committee": "SU",
      "advisory_committee_description": "General, Plastic Surgery",
      "supplement_type": "30-Day Notice",
      "supplement_reason": "Process Change - Manufacturer/Sterilizer/Packager/Supplier",
      "expedited_review_flag": "N",
      "date_received": "2023-02-21",
      "decision_date": "2023-03-22",
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      "decision_code": "OK30",
      "ao_statement": "Change to the stopper, which is a component of the syringe system of the 1.0 and 1.2mL configurations of Revanesse Versa, Revanesse Versa+ with Lidocaine, and Revanesse Lips+ with Lidocaine.",
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