FDA applicant

Damor America, Inc.

Washington, D.C., DC4 decisions1989–19930 recalls

FDA records 4 decisions for Damor America, Inc. (Washington, D.C., DC) from 1989 to 1993: 4 510(k) clearances. Most are in product codes MGQ (Dressing, Wound And Burn, Hydrogel W/Drug…) and FRO (Dressing, Wound, Drug). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Damor America, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Damor America, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Damor America, Inc.

Which product codes does it file in?

What has FDA decided for it lately?