510(k) Report

FDA applicant

Imaging Dynamics Company, Ltd.

Calgary, CA21 decisions2000–20170 recalls

FDA records 21 decisions for Imaging Dynamics Company, Ltd. (Calgary, CA) from 2000 to 2017: 21 510(k) clearances. Most are in product codes KPR (System, X-Ray, Stationary) and MQB (Solid State X-Ray Imager (Flat Panel/Digital…). Since 2016 its 510(k)s took a median of 99 days from receipt to decision, against 30 for FDA’s reviews in the same codes and years. Its devices cite 15 predicates, 12 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Imaging Dynamics Company Limited”, “Imaging Dynamics Corp.”.

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 Imaging Dynamics Company, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

4in 2017

2007: 62011: 12017: 4
2007high 6 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Imaging Dynamics Company, Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Imaging Dynamics Company, Ltd.’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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Other applicant names beginning “Imaging”

FDA records each applicant name separately; these may or may not be the same firm.