FDA applicant

Origin Medical Devices

Newport Beach, CA1 decision2023–20230 recalls

FDA records 1 decision for Origin Medical Devices (Newport Beach, CA) in 2023: 1 510(k) clearance. All are in product code CBK (Ventilator, Continuous, Facility Use). 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, anesthesiology panel, where it files most

How often FDA has decided Origin Medical Devices’s devices, and how often a recall has named them.

FDA decisions per year

1in 2023

2023high 1 (2023) · low 0 (2024)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2023.

FIG. 1 — Origin Medical Devices by year, 2023–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Origin”

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

Origin Medsystems, Inc. 50

Origin Medical Devices

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Origin”