FDA applicant

Orthosource, Inc.

North Hollywood, CA2 decisions2006–20070 recalls

FDA records 2 decisions for Orthosource, Inc. (North Hollywood, CA) from 2006 to 2007: 2 510(k) clearances. Most are in product codes EGS (Handpiece, Contra- And Right-Angle Attachment…) and EFA (Handpiece, Belt And/Or Gear Driven, Dental). 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, dental panel, where it files most

How often FDA has decided Orthosource, 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 — Orthosource, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Orthosource, Inc.

Which product codes does it file in?

What has FDA decided for it lately?