510(k) Report

FDA applicant

Techtrade, LLC

Potomac, MD2 decisions2004–20050 recalls

FDA records 2 decisions for Techtrade, LLC (Potomac, MD) from 2004 to 2005: 2 510(k) clearances. Most are in product codes DQD (Stethoscope, Electronic) and KME (Bedding, Disposable, Medical). Its devices cite 1 predicate, 0 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Techtrade, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • DQDStethoscope, Electronic1decision
  • KMEBedding, Disposable, Medical1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K050097Techno-Scope Visual StethoscopeTechtrade, LLC · 2005
  • K042145Ready-Heat BlanketTechtrade, LLC · 2004

All 2 as Techtrade, LLC →