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Mckinley, Inc.

United StatesFDA applicant, unverified

Devices
7

What Mckinley, Inc. makes

Mckinley, Inc. manufactures infusion pumps, including the Outbound-2 System and disposable syringe infusers like the Outbound 2 Disposable Pump and SP Disposable Infusion Pump. Their portfolio also includes modification kits for existing infusion systems, such as the Accufuser and Accufuser Plus, as well as standalone systems like the Beeline System. Additional products include ambulatory infusion devices like the WalkMed series (300, 350, IC, PCA, and Plus) and patient-controlled analgesia (PCA) systems, including the Motiv, Propolis, and PCA devices.

These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company’s products are listed in the FDA’s 510(k) registry. Mckinley, Inc. is based in the United States.

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

Catalogue7

Newest first, rows 1-7 of 7

Frequently asked questions

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

The registry currently lists 7 devices for Mckinley, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Mckinley, Inc.'s devices?

Among its 7 most recently registered devices, Mckinley, Inc. has devices listed in FDA 510(k) (7 devices).

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

Among its 7 most recently registered devices, the classes recorded for Mckinley, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Mckinley, Inc. include MCKINLEY OUTBOUND-2 SYSTEM, MODIFICATION TO: ACCUFUSER, ACCUFUSER PLUS, STANDARD PROCEDURE KITS, BEELINE MOTIV, PROPOLIS, PCA and WALKMED 300, WALKMED 350, WALKMED IC, WALKMED PCA, WALKMED PLUS.

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