{
  "format": "devicerts.device.v1",
  "cite_as": "Greenlight Moxy Fiber Optic, American Medical Systems. deviCERTS medical device catalogue. https://devicerts.com/devices/greenlight-moxy-fiber-optic-gex (data as of 2026-11-14).",
  "source": {
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    "json_url": "https://devicerts.com/devices/greenlight-moxy-fiber-optic-gex.json",
    "markdown_url": "https://devicerts.com/devices/greenlight-moxy-fiber-optic-gex.md",
    "publisher": "deviCERTS (devicerts.com)",
    "data_sources": [
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    "status_as_of": "2026-11-14",
    "license": "CC BY 4.0",
    "license_url": "https://creativecommons.org/licenses/by/4.0/",
    "license_scope": "The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.",
    "attribution": "DevicErts, https://devicerts.com/devices/greenlight-moxy-fiber-optic-gex",
    "disclaimer": "Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails."
  },
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    "registry_name": "GREENLIGHT MOXY FIBER OPTIC",
    "url": "https://devicerts.com/devices/greenlight-moxy-fiber-optic-gex",
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    "gmdn": [],
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      "device_udi_di": null,
      "date": "2012-06-15",
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    }
  ],
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    {
      "number": "Z-1798-2020",
      "classification": "Class II",
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      "initiated": "2020-03-30",
      "reason": "To reinforce existing instructions within the Directions for Use (DFU) and provide further guidance which will be added to the DFU that may reduce the likelihood of metal cap and fiber tip break temperature related complaints.",
      "applies": "this device",
      "via": "K120870"
    }
  ],
  "eu_market_availability": null,
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