FDA Device Intelligence
Home › AMBLER SURGICAL CORP. › Ambler Surgical

Ambler Surgical

AMBLER SURGICAL CORP. · Model Sinus probe · UDI-DI 00190660128067

KAK Prescription
1
510(k) clearances
7
Adverse events
1
Recalls
92
Facilities

Description

Sinus probe, 7 7/8'', bayonet, graduated beads, probe tip

Recalls

DateFirmReason
2012-08-17Vital Signs Colorado Inc.There is a potential for epistaxis during use of the Disposable General Purpose 9 French Temperature Probe.

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.