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Williams Specialty Products, Inc.

United StatesFDA applicant, unverified

Devices
2

What Williams Specialty Products, Inc. makes

Williams Specialty Products, Inc. manufactures medical adapters and suction devices, including swivel adapters for fluid connections and uterine suction cannulas for clinical procedures.

These products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Swivel Adapter Ref K900642

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Cannula, Suction Uterine Ref K900641

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Williams Specialty Products, Inc. have in the registry?

The registry currently lists 2 devices for Williams Specialty Products, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Williams Specialty Products, Inc.'s devices?

Among its 2 most recently registered devices, Williams Specialty Products, Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do Williams Specialty Products, Inc.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Williams Specialty Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Williams Specialty Products, Inc. in the registry?

The most recently registered devices listed for Williams Specialty Products, Inc. include SWIVEL ADAPTER and CANNULA, SUCTION UTERINE.

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