510(k) Report

FDA applicant

Virtual Imaging, Inc.

Sunnyvale, CA9 decisions1987–20100 recalls

FDA records 9 decisions for Virtual Imaging, Inc. (Sunnyvale, CA) from 1987 to 2010: 9 510(k) clearances. Most are in product codes OWB (Interventional Fluoroscopic X-Ray System) and LLZ (System, Image Processing, Radiological). Its devices cite 17 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Virtual Imaging”.

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 Virtual Imaging, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2007: 12009: 32010: 1
2007high 3 (2009) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Virtual Imaging, 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

Other applicant names beginning “Virtual”

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