FDA applicant

De Medica Mfg., Inc.

Santa Paula, CA3 decisions1988–19880 recalls

FDA records 3 decisions for De Medica Mfg., Inc. (Santa Paula, CA) in 1988: 3 510(k) clearances. Most are in product codes HSB (Rod, Fixation, Intramedullary And Accessories) and JDS (Nail, Fixation, 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 De Medica Mfg., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for De Medica Mfg., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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De Medica Mfg., Inc.

Which product codes does it file in?

What has FDA decided for it lately?