FDA applicant

Newmedical Technology, Inc.

Waukesha, WI3 decisions2003–20050 recalls

FDA records 3 decisions for Newmedical Technology, Inc. (Waukesha, WI) from 2003 to 2005: 3 510(k) clearances. Most are in product codes MDA (Elastomer, Silicone, For Scar Management) and MQN (External Mandibular Fixator And/Or Distractor). Its devices cite 1 predicate, 1 of them its own earlier devices. 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 Newmedical Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Newmedical Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Newmedical Technology, Inc.

Which product codes does it file in?

Which of its devices are cited most?

What has FDA decided for it lately?