FDA applicant

Cedars-Sinai Medical Center

Los Angeles, CA5 decisions2011–20170 recalls

FDA records 5 decisions for Cedars-Sinai Medical Center (Los Angeles, CA) from 2011 to 2017: 5 510(k) clearances. All are in product code KPS (System, Tomography, Computed, Emission). Its devices cite 4 predicates, 2 of them its own earlier devices. 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 Cedars-Sinai Medical Center’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2011high 2 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Cedars-Sinai Medical Center by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Cedars-Sinai Medical Center’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 “Cedars-Sinai”

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

Cedars-Sinai Medical Center: Aim 1 Cedars Medical Center 1

Cedars-Sinai Medical Center

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Cedars-Sinai”