PROPEL VPRO5 ASM-20018

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-08-11 for PROPEL VPRO5 ASM-20018 manufactured by Propel Orthodontics.

Event Text Entries

[82882157] I have two issues to report regarding a medical device by propel orthodontics. The device is called propel vpro5. The first is that it seems this device is being given (sold) to patients by orthodontists for an unapproved purpose. I read that it was approved by the fda as "a device that vibrates to assist clear plastic aligners to fit to a patient's teeth. " instead it was given to me (for additional cost) by an orthodontist to accelerate the movement of teeth during treatment with invisalign aligners. Secondly, this device is held in the mouth by biting and holding. When turned on it produces high frequency vibrations that the patient feels in the jaw and ear. Every time i use this device it immediately causes imbalance and i hear a low pitched humming sound. The imbalance is certainly related to vibrations in the fluid inside the semicircular canals (balance system) of the inner ear. In addition to the obvious imbalance effects, this device should be evaluated for effects on the inner ear cochlear hearing system which would not be immediately obvious to the patient but this could cause permanent hearing damage over time. The product packaging comes with no warnings. I find it unusual that this product would not have been tested for these harmful effects before being sold. The imbalance problem occurs immediately every time i use it. At the very least the patient should be warned about it and instructed to remain seated for the 5 minutes each day that this product is used.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5071559
MDR Report Key6793989
Date Received2017-08-11
Date of Report2017-08-11
Date of Event2017-08-10
Date Added to Maude2017-08-15
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPATIENT
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NamePROPEL VPRO5
Generic NameORTHODONTIC SETTER BAND
Product CodeECR
Date Received2017-08-11
Model NumberASM-20018
Lot Number031317-00001
Device Expiration Date2019-03-13
OperatorLAY USER/PATIENT
Device AvailabilityY
Device Eval'ed by MfgrI
Device Sequence No1
Device Event Key0
ManufacturerPROPEL ORTHODONTICS


Patients

Patient NumberTreatmentOutcomeDate
10 2017-08-11

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.