FDA applicant

Edda Technology, Inc.

Princeton, NJ5 decisions2004–20150 recalls

FDA records 5 decisions for Edda Technology, Inc. (Princeton, NJ) from 2004 to 2015: 5 510(k) clearances. Most are in product codes LLZ (System, Image Processing, Radiological) and JAK (System, X-Ray, Tomography, Computed). Its devices cite 14 predicates, 2 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Edda Technology”.

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

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

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

FDA decisions per year

1in 2015

2007high 1 (2013) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Edda Technology, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?