510(k) Report

FDA applicant

Technology Marketing Group

Maywood, NJ3 decisions1994–19940 recalls

FDA records 3 decisions for Technology Marketing Group (Maywood, NJ) in 1994: 3 510(k) clearances. Most are in product codes LYK (Angioscope) and EOQ (Bronchoscope (Flexible Or Rigid)). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Technology Marketing Group’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Technology Marketing Group since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Technology Marketing Group 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?

  • LYKAngioscope1decision
  • EOQBronchoscope (Flexible Or Rigid)1decision
  • FBNCholedochoscope And Accessories, Flexible/Rigid1decision

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K935834Tas-211/2.3 Ultrathin Flexible EndoscopeTechnology Marketing Group · 19941cites it

What has FDA decided for it lately?

  • K941715Ultathin Flexible EndoscopeTechnology Marketing Group · 1994
  • K942388Tas-(Various) Ultrathin Flexible EndoscopeTechnology Marketing Group · 1994
  • K935834Tas-211/2.3 Ultrathin Flexible EndoscopeTechnology Marketing Group · 1994

All 3 as Technology Marketing Group →