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Padpro, LLC

United StatesFDA applicant, unverified

Devices
5

What Padpro, LLC makes

Padpro, LLC manufactures external defibrillator electrode adapters and pads, including single-use and reusable models designed for compatibility with automated external defibrillators (AEDs). Their products include standalone pads (e.g., Model 2502, Model 2603) and adapter systems (e.g., Model 2516) for connecting electrodes to defibrillators. Additional variants (e.g., Model 2001 series) cater to specific use cases such as pediatric or specialized electrode configurations.

The company’s products fall under Class III regulatory classification in the US, requiring premarket approval (PMA) or a 510(k) clearance via the FDA’s 510(k) pathway. Their devices are listed in the FDA’s 510(k) database, reflecting their authorised status for commercial distribution. The manufacturer is based in the United States.

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

Catalogue5

Newest first, rows 1-5 of 5

Frequently asked questions

How many devices does Padpro, LLC have in the registry?

The registry currently lists 5 devices for Padpro, LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list Padpro, LLC's devices?

Among its 5 most recently registered devices, Padpro, LLC has devices listed in FDA 510(k) (5 devices).

What risk classes do Padpro, LLC's devices fall under?

Among its 5 most recently registered devices, the classes recorded for Padpro, LLC's devices are Class III. Each device page shows its own class and authorisation.

What are the newest devices from Padpro, LLC in the registry?

The most recently registered devices listed for Padpro, LLC include PADPRO, MODEL 2502, PADPRO, MODEL 2603, PADPRO SYSTEM DEFIBRILLATOR ELECTRODE ADAPTERS and PADPRO MODEL 2001, 2001-S, 2001-C, 2001-EPS.

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