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Coeur Laboratories, Inc.

United StatesFDA applicant, unverified

Devices
10

What Coeur Laboratories, Inc. makes

Coeur Laboratories, Inc. manufactures angiographic syringes, control syringes, and related injection components such as front load injector retrofit kits, turrets, and adapters for use in vascular procedures. The company also produces urological catheters, capillary tubes for blood collection, and polyethylene tubing for medical fluid delivery.

The devices listed are classified as Class I and Class II medical devices and are included in the FDA 510(k) registry. Coeur Laboratories, Inc. is based in the United States.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue10

Newest first, rows 1-10 of 10

Frequently asked questions

How many devices does Coeur Laboratories, Inc. have in the registry?

The registry currently lists 10 devices for Coeur Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Coeur Laboratories, Inc.'s devices?

Among its 10 most recently registered devices, Coeur Laboratories, Inc. has devices listed in FDA 510(k) (10 devices).

What risk classes do Coeur Laboratories, Inc.'s devices fall under?

Among its 10 most recently registered devices, the classes recorded for Coeur Laboratories, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Coeur Laboratories, Inc. in the registry?

The most recently registered devices listed for Coeur Laboratories, Inc. include COEUR FRONT LOAD INJECTOR RETROFIT KIT (C859-0002), UROLOGICAL CATHETER, COEURLOCK STERILE DISPOS. ANGIOGRAPHIC and TUBING, POLYETHYLENE.

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