FDA applicant

Syncor International, Inc.

Golden, CO2 decisions2000–20000 recalls

FDA records 2 decisions for Syncor International, Inc. (Golden, CO) in 2000: 2 510(k) clearances. All are in product code KXK (Source, Brachytherapy, Radionuclide). 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, radiology panel, where it files most

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

FDA decisions per year

No FDA decision for Syncor International, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Syncor”

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

Syncor Intl. Corp. 31 Syncor Pharmaceuticals, Inc. 4 Syncor Radiation Management 1

Syncor International, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Syncor”