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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)K120785Substantially equivalent (SESE) · 2012-10-25clearance family

Predicate lineage

Cited as predicate by: K162877, K242718, K250671

Lineage each submission cites, walked transitively (indented = the cited device's own predicates). Extracted from public 510(k) summary text — heuristic, and includes reference devices mentioned alongside true predicates.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2019-07-12NAINo action indicatedCaire, Inc.0
2019-07-12NAINo action indicatedCaire, Inc.0
2019-07-12NAINo action indicatedCaire, Inc0
2019-07-12NAINo action indicatedCaire, Inc0
2017-10-16NAINo action indicatedCaire, Inc.0
2017-10-16NAINo action indicatedCaire, Inc0
2017-10-16NAINo action indicatedCaire, Inc.0
2017-10-16NAINo action indicatedCaire, Inc0
2017-03-16NAINo action indicatedCaire Inc.0
2016-05-16VAIVoluntary action indicatedCaire Inc1
2014-05-13NAINo action indicatedCaire, Inc.0
2014-05-13NAINo action indicatedCaire, Inc.0
2010-10-07VAIVoluntary action indicatedCaire, Inc0
2010-10-07VAIVoluntary action indicatedCaire, Inc0
2010-04-19NAINo action indicatedCaire, Inc0
2010-04-19NAINo action indicatedCaire, Inc.0
2010-04-19NAINo action indicatedCaire, Inc.0
2010-04-19NAINo action indicatedCaire, Inc0
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