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MOBILE-X T100Recalls & reported problems

Denterprise International, Inc. · The device is a diagnostic X-ray system, which is intended to be used by trained dentists and dental X-ray source for producing diagnostic X-ray images using intra-oral image receptors Its use is in adults and pediatric subjects. · Class 2

Data updated Oct 13, 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 00858475006153), received between Feb 15, 2022 and Feb 15, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fire” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Fire1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 15, 2022Fire; Fire

    OPERATOR REPORTED BATTERY FIRE IN MOBILEX HANDHELD PORTABLE X-RAY UNIT SN (B)(4). UNIT WAS IDLE ON COUNTER AT TIME FIRE WAS OBSERVED. NO INJURIES OCCURRED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13538447 ↗

Other Unit, X-Ray, Extraoral With Timer devices

All Unit, X-Ray, Extraoral With Timer devices →

Sources and updates

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