510(k) Report

FDA applicant

Medmark Technologies, LLC

Perkasie, PA1 decision2005–20050 recalls

FDA records 1 decision for Medmark Technologies, LLC (Perkasie, PA) in 2005: 1 510(k) clearance. All are in product code JOW (Sleeve, Limb, Compressible). 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 Medmark Technologies, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medmark Technologies, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medmark Technologies, 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?

  • JOWSleeve, Limb, Compressible1decision

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K050584GS-128 Gradient Compression SystemMedmark Technologies, LLC · 20052cite it

What has FDA decided for it lately?

  • K050584GS-128 Gradient Compression SystemMedmark Technologies, LLC · 2005

The one decision as Medmark Technologies, LLC →

Other applicant names beginning “Medmark”

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

Medmark, Inc. 3