Skip to content
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
  • 510(k)K162856Substantially equivalent (SESE) · 2017-07-18clearance family
Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2014-07-22NAINo action indicatedBonart Co., Ltd.0
2014-07-17VAIVoluntary action indicatedBONART CO. LTD.1
2014-07-17VAIVoluntary action indicatedBONART CO. LTD.1
2011-04-21OAIOfficial action indicatedBONART CO. LTD.0
2011-04-21OAIOfficial action indicatedBonart Co., Ltd.0
2011-04-21OAIOfficial action indicatedBONART CO. LTD.0
Similar devices
Select up to two to place side-by-side with this device.