{
  "companyId": "47637",
  "slug": "stryker-endoscopy-47637",
  "name": "Stryker Endoscopy",
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    "latest": "2026-06-04"
  },
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    "openLast12Months": 0,
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      {
        "resNumber": "Z-1566-2016",
        "productCode": "HIF",
        "status": "Terminated",
        "recallClass": "Class II",
        "initiated": "2016-03-28",
        "reason": "When operating the device in high flow mode (40L/min, 15 mmHg) and connecting to a house gas inlet source, within seconds of insufflating the flow rate would drop to 0L/min and the red Check Gas Supply symbol would appear on the display, immediately suspending insufflation."
      },
      {
        "resNumber": "Z-1831-2015",
        "productCode": "GEI",
        "status": "Terminated",
        "recallClass": "Class II",
        "initiated": "2015-06-03",
        "reason": "Stryker Endoscopy is recalling all non expired SERFAS 90 degree Energy Probes due to reports of fragments of the probe breaking off into the patient."
      },
      {
        "resNumber": "Z-0592-2015",
        "productCode": null,
        "status": "Terminated",
        "recallClass": "Class II",
        "initiated": "2014-11-17",
        "reason": "The parameters provided in the Laparoscopic Manual Instruments Instructions for Use (IFU 1000-401-070 Revision G or prior) do not support the unwrapped Gravity cycle and the Ethylene Oxide cycle sterilization methods"
      },
      {
        "resNumber": "Z-0593-2015",
        "productCode": null,
        "status": "Terminated",
        "recallClass": "Class II",
        "initiated": "2014-11-17",
        "reason": "The parameters provided in the Laparoscopic Manual Instruments Instructions for Use (IFU 1000-401-070 Revision G or prior) do not support the unwrapped Gravity cycle and the Ethylene Oxide cycle sterilization methods"
      },
      {
        "resNumber": "Z-0594-2015",
        "productCode": null,
        "status": "Terminated",
        "recallClass": "Class II",
        "initiated": "2014-11-17",
        "reason": "The parameters provided in the Laparoscopic Manual Instruments Instructions for Use (IFU 1000-401-070 Revision G or prior) do not support the unwrapped Gravity cycle and the Ethylene Oxide cycle sterilization methods"
      }
    ]
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    "countries": [
      "US"
    ]
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      "code": "GCJ",
      "deviceName": "Laparoscope, General & Plastic Surgery",
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      "latest": "2026-02-18",
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    },
    {
      "code": "HRX",
      "deviceName": "Arthroscope",
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      "latest": "2013-01-09",
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    },
    {
      "code": "MBI",
      "deviceName": "Fastener, Fixation, Nondegradable, Soft Tissue",
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    },
    {
      "code": "GEI",
      "deviceName": "Electrosurgical, Cutting & Coagulation & Accessories",
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    },
    {
      "code": "HWC",
      "deviceName": "Screw, Fixation, Bone",
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      "medianReviewDays": 145
    },
    {
      "code": "MAI",
      "deviceName": "Fastener, Fixation, Biodegradable, Soft Tissue",
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      "latest": "2025-05-23",
      "medianReviewDays": 28
    },
    {
      "code": "ERL",
      "deviceName": "Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece",
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    {
      "code": "FGB",
      "deviceName": "Ureteroscope And Accessories, Flexible/Rigid",
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      "medianReviewDays": 153
    },
    {
      "code": "GCX",
      "deviceName": "Apparatus, Suction, Operating-Room, Wall Vacuum Powered",
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    },
    {
      "code": "HET",
      "deviceName": "Laparoscope, Gynecologic (And Accessories)",
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      "latest": "2008-12-16",
      "medianReviewDays": 120
    },
    {
      "code": "HIH",
      "deviceName": "Hysteroscope (And Accessories)",
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      "latest": "2025-07-18",
      "medianReviewDays": 90
    },
    {
      "code": "JDW",
      "deviceName": "Pin, Fixation, Threaded",
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      "latest": "2002-03-15",
      "medianReviewDays": 71
    },
    {
      "code": "FCS",
      "deviceName": "Light, Catheter, Fiberoptic, Glass, Ureteral",
      "clearances": 2,
      "latest": "2015-08-20",
      "medianReviewDays": 63
    },
    {
      "code": "OWN",
      "deviceName": "Confocal Optical Imaging",
      "clearances": 2,
      "latest": "2026-02-12",
      "medianReviewDays": 29
    },
    {
      "code": "EOB",
      "deviceName": "Nasopharyngoscope (Flexible Or Rigid)",
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      "medianReviewDays": 73
    },
    {
      "code": "FAJ",
      "deviceName": "Cystoscope And Accessories, Flexible/Rigid",
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    },
    {
      "code": "FAT",
      "deviceName": "Bougie, Esophageal, And Gastrointestinal, Gastro-Urology",
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    },
    {
      "code": "FLN",
      "deviceName": "Monitor, Electric For Gravity Flow Infusion Systems",
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      "latest": "2002-08-06",
      "medianReviewDays": 25
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    {
      "code": "FSS",
      "deviceName": "Light, Surgical, Floor Standing",
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    {
      "code": "FSY",
      "deviceName": "Light, Surgical, Ceiling Mounted",
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    },
    {
      "code": "GAT",
      "deviceName": "Suture, Nonabsorbable, Synthetic, Polyethylene",
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    },
    {
      "code": "GDW",
      "deviceName": "Staple, Implantable",
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    {
      "code": "GWG",
      "deviceName": "Endoscope, Neurological",
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    {
      "code": "HTY",
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    },
    {
      "code": "IZI",
      "deviceName": "System, X-Ray, Angiographic",
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      "medianReviewDays": 59
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  "productCodesTotal": "28",
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      "kNumber": "K253602",
      "deviceName": "Precision S 4K Sinuscope",
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    },
    {
      "kNumber": "K261037",
      "deviceName": "780 nm SPY Portable Handheld Imaging (SPY-PHI) System",
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    },
    {
      "kNumber": "K260185",
      "deviceName": "1688 4K Camera System with Advanced Imaging Modality; 1788 4K Camera System with Advanced Imaging Modality",
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    },
    {
      "kNumber": "K260108",
      "deviceName": "L12 LED Light Source with AIM",
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    {
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      "deviceName": "Connected OR Hub with Device and Voice Control; SDC4K Information Management System with Device and Voice Control",
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    {
      "kNumber": "K250544",
      "deviceName": "Knotilus+ Biocomposite Knotless Anchor",
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    {
      "kNumber": "K250528",
      "deviceName": "Stryker AlphaVent™ Knotless SP Biocomposite Anchor",
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    "shown": [
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        "name": "STRYKER ENDOSCOPY",
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        "method": "normalised"
      },
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        "name": "Stryker Endoscopy",
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        "method": "normalised"
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      {
        "name": "Stryker Endoscopy",
        "dataset": "device/510k",
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      {
        "name": "Stryker Endoscopy",
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        "name": "Stryker Endoscopy",
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        "method": "normalised"
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    "clearances": "https://api.fda.gov/device/510k.json?search=applicant%3A%22Stryker%20Endoscopy%22",
    "recalls": "https://api.fda.gov/device/recall.json?search=recalling_firm%3A%22Stryker%20Endoscopy%22"
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    {
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  "retrievedAt": "2026-08-11T14:48:53.045Z"
}