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Ljt Surgical, Ltd.

Country not established

Devices
1

What Ljt Surgical, Ltd. makes

Ljt Surgical, Ltd. manufactures the STOPLOSS JONES TUBE, a medical device designed for surgical applications requiring controlled fluid drainage or obstruction prevention.

The STOPLOSS JONES TUBE is classified as a Class II (U) device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Stoploss Jones Tube Ref K140290

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

Frequently asked questions

How many devices does Ljt Surgical, Ltd. have in the registry?

The registry currently lists 1 device for Ljt Surgical, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ljt Surgical, Ltd.'s devices?

Among its 1 most recently registered device, Ljt Surgical, Ltd. has devices listed in FDA 510(k) (1 device).

What are the newest devices from Ljt Surgical, Ltd. in the registry?

The most recently registered devices listed for Ljt Surgical, Ltd. include STOPLOSS JONES TUBE.

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