Midmark 153758-001Recalls & reported problems

Midmark Corporation · The Midmark UltraTrim Dental Chair is intended to provide patient support and positioning during dental exams. · Class 1

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 00841709108952), received between Dec 22, 2023 and Dec 22, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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.

Reports received per month

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Detachment of Device or Device Component1

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.

MalfunctionDec 22, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
THIS REPORT SUMMARIZES AN EVENT THAT WAS REPORTED TO MIDMARK ON DEC 07, 2023 IN WHICH IT WAS STATED THAT THE BACK OF A DENTAL CHAIR DETACHED FROM THE BASE ALLOWING A PATIENT TO SLIDE TO THE FLOOR. THE PATIENT RECEIVED MEDICAL OBSERVATION, AND NO INJURY WAS INDICATED. PER SERVICE NOTE, THE SHOULDER BOLTS THAT HOLD THE BACKREST AT THE SIDE OF THE CHAIR BEHIND THE TOUCH PAD CONTROLS BECAME UNTHREADED. NO FURTHER DETAILS ARE AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18382163 ↗

Device details

UDI-DI	`00841709108952`
Brand	Midmark
Model	153758-001
Company	Midmark Corporation
Product code	NRU · CHAIR, DENTAL, WITHOUT OPERATIVE UNIT
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	—
Single use	No
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Sep 15, 2021

Device type (GMDN): Dental chair, electric

A mains electricity (AC-powered) device designed to support a patient in a seated position to facilitate dental examination, treatment, and/or minor surgery procedures. It is typically adjustable in height to enable healthcare staff to perform procedures while standing. It usually includes head and armrests, a reclining back that may be tilted from a vertical to a horizontal position, and has rotating capabilities; some types can be programmed to several standard positions. Devices intended for dental examination and/or treatment (e.g., lights, irrigation) may be attached as components of the chair, or stand separately as self-supported, wall- or ceiling-mounted units.

Other CHAIR, DENTAL, WITHOUT OPERATIVE UNIT devices

Midmark 153758-003
Midmark Corporation · CHAIR, DENTAL, WITHOUT OPERATIVE UNIT
5 reports

All CHAIR, DENTAL, WITHOUT OPERATIVE UNIT devices →

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 13, 2026 · each report above links to its original FDA record
Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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