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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)K102898Substantially equivalent (SESE) · 2011-12-15clearance family
Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2020-01-23NAINo action indicatedBioteque Taiwan Ltd.0
2020-01-23NAINo action indicatedBioteque Taiwan Ltd.0
2016-12-08VAIVoluntary action indicatedBioteque Taiwan Ltd.1
2016-12-08VAIVoluntary action indicatedBioteque Taiwan Ltd.1
2014-04-03NAINo action indicatedBioteque Taiwan Ltd.0
2014-04-03NAINo action indicatedBioteque Taiwan Ltd.0
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