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Worldwide Medical Technologies, LLC

United StatesFDA applicant, unverified

Devices
15
FDA recalls
1

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What Worldwide Medical Technologies, LLC makes

The company manufactures single-use medical devices for procedural guidance and minimally invasive interventions, including needle guides, biopsy trays, and specialized needles for bone marrow, intracervical, and seed implantation procedures. It also produces systems for brachytherapy, such as seed implant needles and introducer needles, as well as accessories like seeding spacers and pre-loaded strand delivery systems.

These devices are regulated under the FDA’s 510(k) pathway, with most classified as Class I or Class II. The portfolio is listed in the FDA’s 510(k) clearance registry, and the company is based in the United States.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue15

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FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

FDA recall records list 1 recall initiated by Worldwide Medical Technologies, LLC, initiated on 2011-08-12. By recorded status: 1 terminated. The reasons filed fall into these groups: other reasons as filed. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

  • 2011

    • 12 Aug 2011 Z-0040-2012 Unclassified (pre-2012) Terminated Length of the cannula hub is longer and may not permit a fit with the Applicator Distribution: Worldwide Distribution: Nationwide distribution including the states of AR, CO, DE. FL, KY, MD, MI, MN, NY, TX, and VA;…
      Full distribution text Worldwide Distribution: Nationwide distribution including the states of AR, CO, DE. FL, KY, MD, MI, MN, NY, TX, and VA; and the countries of Belgium, and Germany.

Frequently asked questions

How many devices does Worldwide Medical Technologies, LLC have in the registry?

The registry currently lists 15 devices for Worldwide Medical Technologies, LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list Worldwide Medical Technologies, LLC's devices?

Among its 15 most recently registered devices, Worldwide Medical Technologies, LLC has devices listed in FDA 510(k) (15 devices).

What risk classes do Worldwide Medical Technologies, LLC's devices fall under?

Among its 15 most recently registered devices, the classes recorded for Worldwide Medical Technologies, LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for Worldwide Medical Technologies, LLC?

FDA recall records list 1 recall initiated by Worldwide Medical Technologies, LLC, the most recent initiated on 12 Aug 2011. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from Worldwide Medical Technologies, LLC in the registry?

The most recently registered devices listed for Worldwide Medical Technologies, LLC include WORLDWIDE MEDICAL TECHNOLOGIES NEEDLE GUIDE, READI-LOAD SYSTEM, MODEL PSS 1820RL, WORLDWIDE MEDICAL TECHNOLOGIES I TYPE NEEDLE and READI-STRAND, MODEL PSSTRAND.

Generated automatically from registry data and not verified by a human reviewer.