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Travenol Laboratories, S.A.

Country not established

Devices
206

What Travenol Laboratories, S.A. makes

Travenol Laboratories manufactures infusion and administration devices, including burette sets with air control levers, sterile saline and water bottles, solution administration sets, and arterial blood sampling kits. Their portfolio also covers surgical blood-solution administration sets, volumetric infusion pumps, and pediatric ventilator circuits. Additional products include continuous ambulatory peritoneal dialysis (CAPD) transfer sets and disconnect systems, as well as sterile disposable trays for arthrogram procedures and centrifuge bowls.

The company’s devices are regulated under FDA 510(k) clearance, spanning Class I, Class II, and unclassified (U) categories. Their products are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.

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

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Frequently asked questions

How many devices does Travenol Laboratories, S.A. have in the registry?

The registry currently lists 206 devices for Travenol Laboratories, S.A.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Travenol Laboratories, S.A.'s devices?

Among its 50 most recently registered devices, Travenol Laboratories, S.A. has devices listed in FDA 510(k) (50 devices).

What risk classes do Travenol Laboratories, S.A.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for Travenol Laboratories, S.A.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Travenol Laboratories, S.A. in the registry?

The most recently registered devices listed for Travenol Laboratories, S.A. include BURETTE SET WITH AIR CONTROL LEVER, STERILE WATER & SALINE IN PLASTIC BTL., SOLUTION ADMINISTRATION SETS and ARTEOIAL BLOOD SAMPLING KIT 2D9014.

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