FDA applicant

Worldwide Medical Technologies, LLC

Woodbury, CT15 decisions1998–20070 recalls

FDA records 15 decisions for Worldwide Medical Technologies, LLC (Woodbury, CT) from 1998 to 2007: 15 510(k) clearances. Most are in product codes KXK (Source, Brachytherapy, Radionuclide) and KNW (Instrument, Biopsy). 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, radiology panel, where it files most

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

FDA decisions per year

1in 2007

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Worldwide”

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

Worldwide Medical Corp. 9 Worldwide Surgical Gauze 4 Worldwide Dental, Inc. 4

Worldwide Medical Technologies, LLC

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?

Other applicant names beginning “Worldwide”