FDA applicant

The Deca Co.

Costa Mesa, CA9 decisions1982–19870 recalls

FDA records 9 decisions for The Deca Co. (Costa Mesa, CA) from 1982 to 1987: 9 510(k) clearances. Most are in product codes HSB (Rod, Fixation, Intramedullary And Accessories) and JEY (Plate, Bone). 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, orthopedic panel, where it files most

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

FDA decisions per year

No FDA decision for The Deca Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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The Deca Co.

Which product codes does it file in?

What has FDA decided for it lately?