Adverse-event reports (MAUDE)
Read this first: MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.
No adverse-event reports are linked to this device.
Recall history
No recalls linked.
Regulatory clearances
None linked.
Manufacturer compliance record
None in the loaded window.
Similar devices
- "Vista .375"" Non-Vented Surgical Evac Tube" Vista Dental
- "Vista 1/4"" Surgical Evacuation Tip" Vista Dental
- "Vista 1/8"" Surgical Evacuation Tubes" Vista Dental
- 01BA QUALITY ASPIRATORS, INC.
- 01BAT QUALITY ASPIRATORS, INC.
- 02BA QUALITY ASPIRATORS, INC.
- 03BA QUALITY ASPIRATORS, INC.
- 03BAT QUALITY ASPIRATORS, INC.
- 04-90A QUALITY ASPIRATORS, INC.
- 04-90T QUALITY ASPIRATORS, INC.
- 0490AT QUALITY ASPIRATORS, INC.
- 04A QUALITY ASPIRATORS, INC.
Select up to two to place side-by-side with this device.