510(k) Report

FDA product code · Radiology

X-Ray, Computed Tomography, Cone-Beam

SFVClass II21 CFR 892.1750510(k) required2 decisions since 20250 recalls

2 FDA decisions since 2025. 510(k) reviews decided 2021–2025 took a median of 234 days (half between 234 and 234). No recall names this code.

Cone-beam computed tomography produced cross-sectional diagnostic x-ray images of whole body except dental structures.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026 Download the data (CSV)

FIG. A — Illustration, radiology panel

Twenty years of SFV at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FDA decisions per year · SFV

1in 2025

2025: 12026 (partial year): 1
2007high 1 (2025) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · SFV

Too few SFV 510(k)s in any year since 2007 to give a median.

Recalls per year · SFV

No recall names SFV since 2007.

Adverse event reports per year · SFV

No MAUDE report names SFV since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20251—00
20261—0—
FIG. 1 — SFV by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in SFV? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

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Related product codes

Other codes under 21 CFR 892.1750.