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calendar

24,946 catalysts · 5,000 device 510k · 4,728 grant · 4,721 approval · 3,706 8k filing · 2,000 device pma · 2,000 device recall

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2026-08-31: 0 catalysts2026-09-01: 0 catalysts2026-09-02: 0 catalysts2026-09-03: 0 catalysts2026-09-04: 6 catalysts2026-09-05: 0 catalysts2026-09-06: 0 catalysts2026-09-07: 0 catalysts2026-09-08: 0 catalysts2026-09-09: 0 catalysts2026-09-10: 0 catalysts2026-09-11: 0 catalysts2026-09-12: 0 catalysts2026-09-13: 0 catalysts2026-09-14: 0 catalysts2026-09-15: 0 catalysts2026-09-16: 0 catalysts2026-09-17: 0 catalysts2026-09-18: 0 catalysts2026-09-19: 0 catalysts2026-09-20: 0 catalysts2026-09-21: 0 catalysts2026-09-22: 0 catalysts2026-09-23: 2 catalysts2026-09-24: 0 catalysts2026-09-25: 0 catalysts2026-09-26: 0 catalysts2026-09-27: 0 catalysts2026-09-28: 0 catalysts2026-09-29: 0 catalysts2026-09-30: 1 catalyst2026-10-01: 0 catalysts2026-10-02: 0 catalysts2026-10-03: 0 catalysts2026-10-04: 0 catalysts2026-10-05: 0 catalysts2026-10-06: 0 catalysts2026-10-07: 0 catalysts2026-10-08: 2 catalysts2026-10-09: 0 catalysts2026-10-10: 0 catalysts2026-10-11: 0 catalysts2026-10-12: 0 catalysts2026-10-13: 1 catalyst2026-10-14: 1 catalyst2026-10-15: 0 catalysts2026-10-16: 0 catalysts2026-10-17: 0 catalysts2026-10-18: 0 catalysts2026-10-19: 1 catalyst2026-10-20: 2 catalysts2026-10-21: 2 catalysts2026-10-22: 2 catalysts2026-10-23: 1 catalyst2026-10-24: 0 catalysts2026-10-25: 0 catalysts2026-10-26: 1 catalyst2026-10-27: 8 catalysts2026-10-28: 12 catalysts2026-10-29: 21 catalysts2026-10-30: 4 catalysts2026-10-31: 0 catalysts2026-11-01: 0 catalysts2026-11-02: 9 catalysts2026-11-03: 18 catalysts2026-11-04: 22 catalysts2026-11-05: 37 catalysts2026-11-06: 2 catalysts2026-11-07: 0 catalysts2026-11-08: 0 catalysts2026-11-09: 1 catalyst2026-11-10: 0 catalysts2026-11-11: 0 catalysts2026-11-12: 0 catalysts2026-11-13: 0 catalysts2026-11-14: 0 catalysts2026-11-15: 0 catalysts2026-11-16: 0 catalysts2026-11-17: 0 catalysts2026-11-18: 0 catalysts2026-11-19: 0 catalysts2026-11-20: 0 catalysts2026-11-21: 0 catalysts2026-11-22: 0 catalysts2026-11-23: 0 catalysts2026-11-24: 0 catalysts2026-11-25: 0 catalysts2026-11-26: 0 catalysts2026-11-27: 0 catalysts2026-11-28: 0 catalysts2026-11-29: 0 catalysts
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  • device 510k5,000
  • grant4,728
  • approval4,721
  • 8k filing3,706
  • device pma2,000
  • device recall2,000
  • recall1,126
  • device adverse event1,000
  • earnings585
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Nov 3, 2025

    50
    ›Nov 3, 2025device recall306d agoFresenius Kabi USA, LLC device recall (Cls II)Fresenius Kabi USA LLC

    Ivenix Infusion System (IIS), Large Volume Pump. Model Number: LVP-0004. — Reason: Downstream Occlusion alarms may occur during procedures using low flow infusion rates when a check valve* is added to the Ivenix Administration Set. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Alcohol (ALC) Test Saliva — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Gut Microbiome Test XL — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Pet Allergy Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoOrthofix U.S. LLC device recall (Cls III)

    Brand Name: Forza" Ti Spacer System Product Name: Forza" Ti Spacer System Model/Catalog Number: 38-2006SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 6H; 38-2007SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 7H; 38-2008SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 8H; 38-2009SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 9H; 38-2010SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 10H; 38-2011SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 11H; 38-2012SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 12H; 38-2013SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 13H; 38-2014SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 14H; 38-2106SP FORZA Ti Spacer, Straight, 0¿, 9W x 27L x 6H; 38-2107SP FORZA Ti Spacer, Straight, 0¿, 9W x 27L x 7H; 38-2108SP FORZA Ti Spacer, Straight, 0¿, 9W x 27L x 8H; 38-2109SP FORZA Ti Spacer, Straight, 0¿, 9W x 27L x 9H; 38-2110SP FORZA Ti Spacer, Straight, 0¿, 9W x 27L x 10H; 38-2111SP FORZA Ti Spacer, Straight, 0¿, 9W x 27L x 11H; 38-2112SP FORZA Ti Spacer, Straight, 0¿, 9W x 27L x 12H; 38-2113SP FORZA Ti Spacer, Straight, 0¿, 9W x 27L x 13H; 38-2114SP FORZA Ti Spacer, Straight, 0¿, 9W x 27L x 14H; 38-2206SP FORZA Ti Spacer, Straight, 0¿, 11W x 27L x 6H; 38-2207SP FORZA Ti Spacer, Straight, 0¿, 11W x 27L x 7H; 38-2208SP FORZA Ti Spacer, Straight, 0¿, 11W x 27L x 8H; 38-2209SP FORZA Ti Spacer, Straight, 0¿, 11W x 27L x 9H; 38-2210SP FORZA Ti Spacer, Straight, 0¿, 11W x 27L x 10H; 38-2211SP FORZA Ti Spacer, Straight, 0¿, 11W x 27L x 11H; 38-2212SP FORZA Ti Spacer, Straight, 0¿, 11W x 27L x 12H; 38-2213SP FORZA Ti Spacer, Straight, 0¿, 11W x 27L x 13H; 38-2214SP FORZA Ti Spacer, Straight, 0¿, 11W x 27L x 14H; 38-2309SP FORZA Ti Spacer, Straight, 8¿, 11W x 27L x 9H; 38-2310SP FORZA Ti Spacer, Straight, 8¿, 11W x 27L x 10H; 38-2311SP FORZA Ti Spacer, Straight, 8¿, 11W x 27L x 11H; 38-2312SP FORZA Ti Spacer, Straight, 8¿, 11W x 27L x 12H; 38-2313SP FORZA Ti Spacer, Straight, 8¿, 11W x 27L x 13H; 38-2314SP FORZA Ti Spacer, Straight, 8¿, 11W x 27L x 14H; 38-2508SP FORZA Ti Spacer, Straight, 8¿, 9W x 23L x 8H; 38-2509SP FORZA Ti Spacer, Straight, 8¿, 9W x 23L x 9H; 38-2510SP FORZA Ti Spacer, Straight, 8¿, 9W x 23L x 10H; 38-2511SP FORZA Ti Spacer, Straight, 8¿, 9W x 23L x 11H; 38-2512SP FORZA Ti Spacer, Straight, 8¿, 9W x 23L x 12H; 38-2513SP FORZA Ti Spacer, Straight, 8¿, 9W x 23L x 13H; 38-2514SP FORZA Ti Spacer, Straight, 8¿, 9W x 23L x 14H; 38-3206SP FORZA Ti Spacer, Straight, 0¿, 11W x 31L x 6H; 38-3207SP FORZA Ti Spacer, Straight, 0¿, 11W x 31L x 7H; 38-3208SP FORZA Ti Spacer, Straight, 0¿, 11W x 31L x 8H; 38-3209SP FORZA Ti Spacer, Straight, 0¿, 11W x 31L x 9H; 38-3210SP FORZA Ti Spacer, Straight, 0¿, 11W x 31L x 10H; 38-3211SP FORZA Ti Spacer, Straight, 0¿, 11W x 31L x 11H; 38-3212SP FORZA Ti Spacer, Straight, 0¿, 11W x 31L x 12H; 38-3213SP FORZA Ti Spacer, Straight, 0¿, 11W x 31L x 13H; 38-3214SP FORZA Ti Spacer, Straight, 0¿, 11W x 31L x 14H; 38-3409SP FORZA Ti Spacer, Straight, 8¿, 11W x 31L x 9H; 38-3410SP FORZA Ti Spacer, Straight, 8¿, 11W x 31L x 10H; 38-3411SP FORZA Ti Spacer, Straight, 8¿, 11W x 31L x 11H; 38-3412SP FORZA Ti Spacer, Straight, 8¿, 11W x 31L x 12H; — Reason: Labeling contains claims that are not consistently present. — Status: Ongoing

    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Urinary Tract Infection Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Lactose Intolerance Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    PSA Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Gut Microbiome Test Small — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    8 in 1 STI Test Kit — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Akkermansia Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Food Intolerance Test Medium — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGE Healthcare GmbH device recall (Cls II)

    GE HealthCare ViewPoint 6, Catalog Number H47601AA; Radiological image processing system — Reason: GE HealthCare has become aware that the Patient History tab in ViewPoint 6 versions 6.15.3 and 6.15.4 ultrasound software may not include complete patient medical history information. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Food Sensitivity Test Large — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoFresenius Kabi USA, LLC device recall (Cls I)Fresenius Kabi USA LLC

    IVENIX INFUSION SYSTEM, LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Dual Y-Site (Qty 25). Large Volume Infusion Pump Administration Set. — Reason: Incorrect assembly of specific lot of LVP Primary Administration Set that could result in serious patient injury. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Mycotoxin Panel Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Food Sensitivity Test Small — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Allergy test Small — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Peptic Ulcer Test (H, pylori) — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Heavy Metals Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Fructose Intolerance Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Trichomonas Vaginalis test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    SIBO Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Intestinal Worms Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    D-Dimer Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Diabetes HbA1c Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Candida Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Syphilis Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Iodine Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    MPOX Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    GI Microbiome Profile Small — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoOrthofix U.S. LLC device recall (Cls III)

    Brand Name: CONSTRUX" Mini Ti Spacer System Product Name: CONSTRUX" Mini Ti Spacer System Model/Catalog Number: 37-6005SP 12mm W X 12mm L, 5mm H, 5¿ Lordotic 37-6005SP 12mm W X 12mm L, 5mm H, 5¿ Lordotic 37-6005SP 12mm W X 12mm L, 5mm H, 5¿ Lordotic 37-6006SP 12mm W X 12mm L, 6mm H, 5¿ Lordotic 37-6006SP 12mm W X 12mm L, 6mm H, 5¿ Lordotic 37-6006SP 12mm W X 12mm L, 6mm H, 5¿ Lordotic 37-6007SP 12mm W X 12mm L, 7mm H, 5¿ Lordotic 37-6007SP 12mm W X 12mm L, 7mm H, 5¿ Lordotic 37-6007SP 12mm W X 12mm L, 7mm H, 5¿ Lordotic 37-6008SP 12mm W X 12mm L, 8mm H, 5¿ Lordotic 37-6008SP 12mm W X 12mm L, 8mm H, 5¿ Lordotic 37-6008SP 12mm W X 12mm L, 8mm H, 5¿ Lordotic 37-6009SP 12mm W X 12mm L, 9mm H, 5¿ Lordotic 37-6009SP 12mm W X 12mm L, 9mm H, 5¿ Lordotic 37-6009SP 12mm W X 12mm L, 9mm H, 5¿ Lordotic 37-6010SP 12mm W X 12mm L, 10mm H, 5¿ Lordotic 37-6010SP 12mm W X 12mm L, 10mm H, 5¿ Lordotic 37-6010SP 12mm W X 12mm L, 10mm H, 5¿ Lordotic 37-6011SP 12mm W X 12mm L, 11mm H, 5¿ Lordotic 37-6011SP 12mm W X 12mm L, 11mm H, 5¿ Lordotic 37-6011SP 12mm W X 12mm L, 11mm H, 5¿ Lordotic 37-6012SP 12mm W X 12mm L, 12mm H, 5¿ Lordotic 37-6012SP 12mm W X 12mm L, 12mm H, 5¿ Lordotic 37-6012SP 12mm W X 12mm L, 12mm H, 5¿ Lordotic 37-6105SP 12mm W X 12mm L, 5mm H, Parallel 37-6105SP 12mm W X 12mm L, 5mm H, Parallel 37-6105SP 12mm W X 12mm L, 5mm H, Parallel 37-6106SP 12mm W X 12mm L 6mm H, Parallel 37-6106SP 12mm W X 12mm L 6mm H, Parallel 37-6106SP 12mm W X 12mm L 6mm H, Parallel 37-6107SP 12mm W X 12mm L, 7mm H, Parallel 37-6107SP 12mm W X 12mm L, 7mm H, Parallel 37-6107SP 12mm W X 12mm L, 7mm H, Parallel 37-6108SP 12mm W X 12mm L, 8mm H, Parallel 37-6108SP 12mm W X 12mm L, 8mm H, Parallel 37-6108SP 12mm W X 12mm L, 8mm H, Parallel 37-6109SP 12mm W X 12mm L, 9mm H, Parallel 37-6109SP 12mm W X 12mm L, 9mm H, Parallel 37-6109SP 12mm W X 12mm L, 9mm H, Parallel 37-6110SP 12mm W X 12mm L, 10mm H, Parallel 37-6110SP 12mm W X 12mm L, 10mm H, Parallel 37-6110SP 12mm W X 12mm L, 10mm H, Parallel 37-6111SP 12mm W X 12mm L, 11mm H, Parallel 37-6111SP 12mm W X 12mm L, 11mm H, Parallel 37-6111SP 12mm W X 12mm L, 11mm H, Parallel 37-6112SP 12mm W X 12mm L, 12mm H, Parallel 37-6112SP 12mm W X 12mm L, 12mm H, Parallel 37-6112SP 12mm W X 12mm L, 12mm H, Parallel 37-6206SP 12mm W X 12mm L, 6mm H, 10¿ Lordotic 37-6206SP 12mm W X 12mm L, 6mm H, 10¿ Lordotic 37-6206SP 12mm W X 12mm L, 6mm H, 10¿ Lordotic 37-6207SP 12mm W X 12mm L, 7mm H, 10¿ Lordotic 37-6207SP 12mm W X 12mm L, 7mm H, 10¿ Lordotic 37-6207SP 12mm W X 12mm L, 7mm H, 10¿ Lordotic 37-6208SP 12mm W X 12mm L, 8mm H, 10¿ Lordotic 37-6208SP 12mm W X 12mm L, 8mm H, 10¿ Lordotic 37-6208SP 12mm W X 12mm L, 8mm H, 10¿ Lordotic 37-6209SP 12mm W X 12mm L, 9mm H, 10¿ Lordotic 37-6209SP 12mm W X 12mm L, 9mm H, 10¿ Lordotic 37-6209SP 12mm W X 12mm L, 9mm H, 10¿ Lordotic 37-6210SP 12mm W X 12mm L, 10mm H, 10¿ Lordotic 37-6210SP 12mm W X 12mm L, 10mm H, 10¿ Lordotic 37-6210SP 12mm W X 12mm L, 10mm H, 10¿ Lordotic 37-6211SP 12mm W X 12mm L, 11mm H, 10¿ Lordotic 37-6211SP 12mm W X 12mm L, 11mm H, 10¿ Lordotic 37-6211SP 12mm W X 12mm L, 11mm H, 10¿ Lordotic — Reason: Labeling contains claims that are not consistently present. — Status: Ongoing

    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Parasite Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Sperm Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    DHEA Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Serotonin Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Female Fertility Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Gut Microbiome Test Mega — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoOrthofix U.S. LLC device recall (Cls III)

    Brand Name: CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PTC Spacer System Model/Catalog Number: 37-3106SP 12mm W X 12mm L, 6mm H, Parallel; 37-3107SP 12mm W X 12mm L, 7mm H, Parallel; 37-3108SP 12mm W X 12mm L, 8mm H, Parallel; 37-3109SP 12mm W X 12mm L, 9mm H, Parallel; 37-3110SP 12mm W X 12mm L, 10mm H, Parallel; 37-3111SP 12mm W X 12mm L, 11mm H, Parallel; 37-3112SP 12mm W X 12mm L, 12mm H, Parallel; 37-3113SP 12mm W X 12mm LW, 13mm H, Parallel; 37-3114SP 12mm W X 12mm WL, 14mm H, Parallel; 37-3006SP 12mm W X 12mm L, 6mm H, 5¿ Lordotic; 37-3007SP 12mm W X 12mm L, 7mm H, 5¿ Lordotic; 37-3008SP 12mm W X 12mm L, 8mm H, 5¿ Lordotic; 37-3009SP 12mm WL X 12mm L, 9mm H, 5¿ Lordotic; 37-3010SP 12mm W X 12mm L, 10mm H, 5¿ Lordotic; 37-3011SP 12mm W X 12mm L, 11mm H, 5¿ Lordotic; 37-3012SP 12mm W X 12mm L, 12mm H, 5¿ Lordotic; 37-3013SP 12mm W X 12mm L, 13mm H, 5¿ Lordotic; 37-3014SP 12mm W X 12mm L, 14mm H, 5¿ Lordotic; 37-3207SP 12mm W X 12mm L, 7mm H, 10¿ Lordotic; 37-3208SP 12mm W X 12mm L, 8mm H, 10¿ Lordotic; 37-3209SP 12mm W X 12mm L, 9mm H, 10¿ Lordotic; 37-3210SP 12mm W X 12mm L, 10mm H, 10¿ Lordotic; 37-3211SP 12mm W X 12mm L, 11mm H, 10¿ Lordotic; 37-3212SP 12mm W X 12mm L, 12mm H, 10¿ Lordotic; 37-4106SP 15mm W X 12mm L, 6mm H, Parallel; 37-4107SP 15mm W X 12mm L, 7mm H, Parallel; 37-4108SP 15mm W X 12mm L, 8mm H, Parallel; 37-4109SP 15mm W X 12mm L, 9mm H, Parallel; 37-4110SP 15mm W X 12mm L, 10mm H, Parallel; 37-4111SP 15mm W X 12mm L, 11mm H, Parallel; 37-4112SP 15mm W X 12mm L, 12mm H, Parallel; 37-4113SP 15mm W X 12mm L, 13mm H, Parallel; 37-4114SP 15mm W X 12mm L, 14mm H, Parallel; 37-4006SP 15mm W X 12mm L, 6mm H, 5¿ Lordotic; 37-4007SP 15mm W X 12mm L, 7mm H, 5¿ Lordotic; 37-4008SP 15mm W X 12mm L, 8mm H, 5¿ Lordotic; 37-4009SP 15mm W X 12mm L, 9mm H, 5¿ Lordotic; 37-4010SP 15mm W X 12mm L, 10mm H, 5¿ Lordotic; 37-4011SP 15mm W X 12mm L, 11mm H, 5¿ Lordotic; 37-4012SP 15mm W X 12mm L, 12mm H, 5¿ Lordotic; 37-4013SP 15mm W X 12mm L, 13mm H, 5¿ Lordotic; 37-4014SP 15mm W X 12mm L, 14mm H, 5¿ Lordotic; 37-4207SP 15mm W X 12mm L, 7mm H, 10¿ Lordotic; 37-4208SP 15mm W X 12mm L, 8mm H, 10¿ Lordotic; 37-4209SP 15mm W X 12mm L, 9mm H, 10¿ Lordotic; 37-4210SP 15mm W X 12mm L, 10mm H, 10¿ Lordotic; 37-4211SP 15mm W X 12mm L, 11mm H, 10¿ Lordotic; 37-4212SP 15mm W X 12mm L, 12mm H, 10¿ Lordotic; 37-5106SP 15mm W X 15mm L, 6mm H, Parallel; 37-5107SP 15mm W X 15mm L, 7mm H, Parallel 37-5108SP 15mm W X 15mm L, 8mm H, Parallel; 37-5109SP 15mm W X 15mm L, 9mm H, Parallel; 37-5110SP 15mm W X 15mm L, 10mm H, Parallel; 37-5111SP 15mm W X 15mm L, 11mm H, Parallel; 37-5112SP 15mm W X 15mm L, 12mm H, Parallel; 37-5113SP 15mm W X 15mm L, 13mm H, Parallel; 37-5114SP 15mm W X 15mm L, 14mm H, Parallel; 37-5006SP 15mm W X 15mm L, 6mm H, 5¿ Lordotic; 37-5007SP 15mm W X 15mm L, 7mm H, 5¿ Lordotic; 37-5008SP 15mm W X 15mm L, 8mm H, 5¿ Lordotic; 37-5009SP 15mm W X 15mm L, 9mm H, 5¿ Lordotic; 37-5010SP 15mm W X 15mm L, 10mm H, 5¿ Lordotic; 37-5011SP 15mm W X 15mm L, 11mm H, 5¿ Lordotic; 37-5012SP 15mm W X 15mm L, 12mm H, 5¿ Lordotic; 37-5013SP 15mm W X 15mm L, 13mm H, 5¿ Lordotic; 37-5014SP 15mm W X 15mm L, 14mm H, 5¿ Lordotic; 37-5207SP 15mm W X 15mm L, 7mm H, 10¿ Lordotic; 37-5208SP 15mm W X 15mm L, 8mm H, 10¿ Lordotic; 37-5209SP 15mm W X 15mm LW, 9mm H, 10¿ Lordotic; 37-5210SP 15mm W X 15mm L, 10mm H, 10¿ Lordotic; 37-5211SP 15mm W X 15mm L, 11mm H, 10¿ Lordotic; 37-5212SP 15mm W X 15mm L, 12mm H, 10¿ Lordotic; — Reason: Labeling contains claims that are not consistently present. — Status: Ongoing

    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Food Allergy Panel Test (IgE) — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Food Intolerance Test Large — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    NAD Profile Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

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    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Vitamin D2 and D3 Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Leaky Gut Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

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    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Kidney Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

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    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    2 in 1 Trichomonas / Gardnerella Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Menopause (FSH) 2 Tests — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

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    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Blood Type Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    3 in 1 STI Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall306d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Biological Age & Longevity Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

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