{
  "format": "devicerts.device.v1",
  "cite_as": "Intimol, Dlc Laboratories, Inc. deviCERTS medical device catalogue. https://devicerts.com/devices/intimol-nuc (data as of 2026-11-14).",
  "source": {
    "canonical_url": "https://devicerts.com/devices/intimol-nuc",
    "json_url": "https://devicerts.com/devices/intimol-nuc.json",
    "markdown_url": "https://devicerts.com/devices/intimol-nuc.md",
    "publisher": "deviCERTS (devicerts.com)",
    "data_sources": [
      {
        "registry": "FDA 510(k)",
        "url": "https://open.fda.gov/apis/device/510k/"
      }
    ],
    "registry_records_last_synced": "2026-10-22",
    "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/intimol-nuc",
    "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."
  },
  "device": {
    "name": "Intimol",
    "registry_name": "INTIMOL",
    "url": "https://devicerts.com/devices/intimol-nuc",
    "manufacturer": {
      "name": "Dlc Laboratories, Inc.",
      "url": "https://devicerts.com/manufacturers/dlc-laboratories-inc",
      "country": null,
      "country_basis": null,
      "fda_registration_country": "United States"
    },
    "status": {
      "state": "active",
      "label": "Active",
      "detail": "United States"
    },
    "classification": [
      {
        "class": "Class II",
        "system": "US FDA"
      }
    ],
    "identifiers": [
      {
        "label": "510(k) Number",
        "values": [
          {
            "value": "K061466",
            "registries": [
              "FDA 510(k)"
            ]
          }
        ]
      }
    ],
    "product_codes": [
      "NUC"
    ],
    "emdn": [],
    "gmdn": [],
    "description": {
      "text": "Intimol is a personal lubricant classified as an obstetrics and gynecology device. It is designed to provide lubrication for personal use.\n\nThis device is regulated under FDA 510(k) clearance number K061466. It is categorized as a Class 2 medical device.",
      "ai_generated": true,
      "generated_on": "2026-10-06",
      "note": "Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data is the record."
    },
    "noindex": false
  },
  "authorizations": [
    {
      "registry": "510(k)",
      "region": "United States",
      "type": "FDA 510(k)",
      "number": "K061466",
      "number_label": null,
      "device_udi_di": null,
      "date": "2006-12-04",
      "date_kind": "decision",
      "decision_code": "SESE",
      "expires": null,
      "withdrawn": null,
      "status": "Active",
      "status_note": null,
      "derived_from_gudid": false
    }
  ],
  "no_longer_listed_by": [],
  "certificates": [],
  "recalls": [],
  "eu_market_availability": null,
  "properties": [
    {
      "group": "Identifiers",
      "fields": [
        {
          "label": "510(k) Number",
          "values": [
            {
              "value": "K061466",
              "registries": [
                "FDA 510(k)"
              ]
            }
          ]
        },
        {
          "label": "FDA product code",
          "values": [
            {
              "value": "NUC",
              "registries": [
                "FDA 510(k)"
              ]
            }
          ]
        }
      ]
    },
    {
      "group": "Classification",
      "fields": [
        {
          "label": "Device class",
          "values": [
            {
              "value": "Class II",
              "registries": [
                "FDA 510(k)"
              ]
            }
          ]
        },
        {
          "label": "Regulation",
          "values": [
            {
              "value": "21 CFR Part 884.5300",
              "registries": [
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            }
          ]
        },
        {
          "label": "Advisory committee",
          "values": [
            {
              "value": "Obstetrics/Gynecology",
              "registries": [
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              ]
            }
          ]
        },
        {
          "label": "FDA decision",
          "values": [
            {
              "value": "SESE",
              "registries": [
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              ]
            }
          ]
        }
      ]
    }
  ]
}