510(k) Report

FDA applicant

Apex Imaging Corp.

Duarte, CA1 decision1987–19870 recalls

FDA records 1 decision for Apex Imaging Corp. (Duarte, CA) in 1987: 1 510(k) clearance. All are in product code DSF (Recorder, Paper Chart). 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 Apex Imaging Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Apex Imaging Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Apex Imaging Corp.’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 “Apex”

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