810nm 200mW Standard Tip 2.3Recalls & reported problems
Thor Photomedicine Limited · S2092 810nm 200mW Standard Tip · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05060494130220), received between Mar 20, 2025 and Mar 20, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Unintended Power Up” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Unintended Power Up1
Patient problems
- Eye Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 20, 2025Unintended Power Up; Unintended Power Up
THE TRIGGER POINT PROBE HAS BEEN TURNING ON INVOLUNTARILY WHEN THE CONTROL UNIT IS SWITCHED ON. THE LASER WILL START WITHOUT MANUALLY PRESSING THE ON/OFF BUTTON.
Patient problems: Eye Injury
MAUDE report 21653049 ↗
Other Lamp, Infrared, Therapeutic Heating devices
- NovoTHOR 3.0Thor Photomedicine Limited · Lamp, Infrared, Therapeutic Heating2 recalls0 reports
- NovoTHOR XL 3.0Thor Photomedicine Limited · Lamp, Infrared, Therapeutic Heating2 recalls0 reports
- NovoTHOR PRX 3.0Thor Photomedicine Limited · Lamp, Infrared, Therapeutic Heating1 recall0 reports
- NovoTHOR Gen 3.0 Reg PRXThor Photomedicine Limited · Lamp, Infrared, Therapeutic Heating1 recall0 reports
- 810nm 1W Cluster (5x200mW) 2.0Thor Photomedicine Limited · Lamp, Infrared, Therapeutic Heating3 reports
- CHATTANOOGA 27812Djo, LLC · Lamp, infrared, therapeutic heating3 reports
- CHATTANOOGA 27840Djo, LLC · Lamp, infrared, therapeutic heating2 reports
- LightForce FXi LTC-1500Litecure LLC · Lamp, Infrared, Therapeutic Heating1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page