FDA applicant

Devcom, Inc.

Paoli, PA6 decisions1985–19900 recalls

FDA records 6 decisions for Devcom, Inc. (Paoli, PA) from 1985 to 1990: 6 510(k) clearances. Most are in product codes KPR (System, X-Ray, Stationary) and JDL (Prosthesis, Hip, Semi-Constrained (Metal…). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Devcom, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Devcom, Inc.

Which product codes does it file in?

What has FDA decided for it lately?