{
  "title": "FDA 510(k) clearances and device recalls by specialty, 2026",
  "as_of": "2026-11-04",
  "total": 764,
  "summary": "As of 2026-11-04, Zalwin tracks 764 FDA device records. The largest group is Other with 399 (52% of the total). Figures are computed from public records and refresh automatically.",
  "rows": [
    {
      "group": "Other",
      "records": 399
    },
    {
      "group": "Radiology",
      "records": 56
    },
    {
      "group": "Orthopedic",
      "records": 53
    },
    {
      "group": "Cardiovascular",
      "records": 52
    },
    {
      "group": "General & Plastic Surgery",
      "records": 44
    },
    {
      "group": "Dental",
      "records": 32
    },
    {
      "group": "Gastroenterology & Urology",
      "records": 27
    },
    {
      "group": "Neurology",
      "records": 23
    },
    {
      "group": "Microbiology",
      "records": 21
    },
    {
      "group": "Clinical Chemistry",
      "records": 15
    },
    {
      "group": "General Hospital",
      "records": 14
    },
    {
      "group": "Anesthesiology",
      "records": 12
    },
    {
      "group": "Obstetrics & Gynecology",
      "records": 9
    },
    {
      "group": "Ophthalmic",
      "records": 7
    }
  ]
}