FDA applicant

Ingress Technologies, Inc.

Phoenix, AZ1 decision1989–19890 recalls

FDA records 1 decision for Ingress Technologies, Inc. (Phoenix, AZ) in 1989: 1 510(k) clearance. All are in product code DXP (Transducer, Vessel Occlusion). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Ingress Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ingress Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ingress Technologies, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Ingress Technologies, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Ingress Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?