Home › PATH medical GmbH › Sentiero Advanced

Sentiero Advanced

PATH medical GmbH · Model 100340-SC-AT-LT · UDI-DI 04260223145261

GWJ EWO Prescription

510(k) clearances

119

Adverse events

Recalls

Facilities

Description

100340-SC-AT Sentiero Advanced ABR and TEOAE Screening Set Content: 1. Case AN100503 2. Inlay Sentiero AN100677 3. USB data cable AN100089 4. Path electrodes: 30 pcs. / bag. Each bag contains 10 sets of 3 pcs. AN 100468 5. Sentiero Advanced device with touchscreen AN100360 6. ABR electrode cable AN100307 7. Probe EP-LT AN101021 8. Accessory box EP-LT AN101043 9. ABR Quick SW AN100337-Quick 10. TEOAE Quick SW AN100109-Quick 11. Mira PC Patient Management SW AN100116 12. Label Printer SW AN100414 13. Power Supply Sentiero Advanced US AN101016+AN100993-USA

Recalls

Date	Firm	Reason
2025-11-06	PATH	Following a component change in the DPOAE probe (speaker replacement), technical distortions may occur at high stimulus levels combined with unusually low OAE amplitude acceptance
2019-05-28	GN Otometrics	There is a risk to the healthcare professional or patient of exposure to undergrounded electrical surfaces which may result in an electrical shock.
2010-06-04	Natus Medical Inc	There is insufficient evidence to support any claims for safety and efficacy on the SonaMed Clarity devices.
2008-10-21	Intelligent 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 key Read 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.