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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

    Predicate lineage

    K080950

    Cited as predicate by: K110179, K200088, K201290, K202648, K210002, K213622, K230701, K232786, K241488, K243828

    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
    2019-11-21VAIVoluntary action indicatedOtto Bock Healthcare Products GmbH2
    2012-10-19VAIVoluntary action indicatedOtto Bock Healthcare Products GmbH5
    2012-10-17VAIVoluntary action indicatedOtto Bock Healthcare Products GmbH3
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