FDA applicant

Technology Delivery Systems, Inc.

New Orleans, LA3 decisions2002–20120 recalls

FDA records 3 decisions for Technology Delivery Systems, Inc. (New Orleans, LA) from 2002 to 2012: 3 510(k) clearances. Most are in product codes FGB (Ureteroscope And Accessories, Flexible/Rigid) and GEX (Powered Laser Surgical Instrument). Its devices cite 2 predicates, 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, gastroenterology and urology panel, where it files most

How often FDA has decided Technology Delivery Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2012

2007high 1 (2012) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Technology Delivery Systems, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?