FDA applicant

Ludlow Technical Products

Chicopee, MA5 decisions1993–19990 recalls

FDA records 5 decisions for Ludlow Technical Products (Chicopee, MA) from 1993 to 1999: 5 510(k) clearances. Most are in product codes NAE (Dressing, Wound, Hydrogel Without Drug And/Or…) and FMT (Warmer, Infant Radiant). 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, general and plastic surgery panel, where it files most

How often FDA has decided Ludlow Technical Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ludlow Technical Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Ludlow”

FDA records each applicant name separately; these may or may not be the same firm.

The Ludlow Company LP 3 Ludlow Corp., Technical Papers Division 1

Ludlow Technical Products

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Ludlow”