FDA applicant

Right Dose, Inc.

Port Washington, NY1 decision2017–20170 recalls

FDA records 1 decision for Right Dose, Inc. (Port Washington, NY) in 2017: 1 510(k) clearance. All are in product code JAK (System, X-Ray, Tomography, Computed). 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 Right Dose, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2017high 1 (2017) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — Right Dose, Inc. by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Right Dose, Inc.

Which product codes does it file in?

What has FDA decided for it lately?