FDA Device Intelligence
HomeOTODYNAMICS LIMITED › ABR Electrode Cable V2 (SNAP) for Otoport V2/Pro

ABR Electrode Cable V2 (SNAP) for Otoport V2/Pro

OTODYNAMICS LIMITED · Model OPRO-SEC · UDI-DI 05060396172373

GWJ
1
510(k) clearances
119
Adverse events
4
Recalls
57
Facilities

Description

ABR electrodes cable for use with 4mm SNAP electrodes, length 47"/1.2m, Red/Black/White color coding, right-angle yellow 4-pin plug, for use with Otoport Pro

Recalls

DateFirmReason
2025-11-06PATHFollowing a component change in the DPOAE probe (speaker replacement), technical distortions may occur at high stimulus levels combined with unusually low OAE amplitude acceptance
2019-05-28GN OtometricsThere is a risk to the healthcare professional or patient of exposure to undergrounded electrical surfaces which may result in an electrical shock.
2010-06-04Natus Medical IncThere is insufficient evidence to support any claims for safety and efficacy on the SonaMed Clarity devices.
2008-10-21Intelligent Hearing Systems Corp.This was a marketing correction mandated by the United States Food and Drug Administration (USFDA). USFDA notified Intelligent Hearing Systems that 501(k) premarket notification ap

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.