FDA applicant

Camsight Co., Inc.

Los Angeles, CA4 decisions1999–20070 recalls

FDA records 4 decisions for Camsight Co., Inc. (Los Angeles, CA) from 1999 to 2007: 4 510(k) clearances. Most are in product codes MUH (System, X-Ray, Extraoral Source, Digital) and EIA (Unit, Operative Dental). No recall is linked to its devices.

FDA’s records also spell it “Camsight, Inc.”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

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

FDA decisions per year

1in 2007

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Camsight Co., Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Camsight Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?