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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
InitiatedRecall #ClassStatusReasonQuantityLink basis
2021-09-07Z-0031-2022Class IITerminatedError in the device firmware results in the inaccurate detection of device position.Distribution: US Nationwide distribution in the states of OH, IL, GA, IA, CA, PA, NM, MI, SD.128 unitscode info di
Regulatory clearances

    Predicate lineage

    K082113

    Cited as predicate by: K124062, K143272, K163665, K192469, K192624, K242290

    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

    None in the loaded window.

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