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Schneider-Shilley (USA)

Country not established

Devices
9

What Schneider-Shilley (USA) makes

The company produces modified medical devices for vascular and catheter-based procedures, including inflation syringes, pressure manometers, and flushing catheters. Their portfolio also includes peripheral dilatation catheters, puncture instruments, and wire torque tools designed for interventional radiology and peripheral vascular access. These devices are tailored for use in angioplasty and catheter-based interventions, ensuring compatibility with existing medical systems.

All listed devices fall under Class II regulatory classification in the US, requiring 510(k) clearance through the FDA. The company’s products are registered under the US Food and Drug Administration’s 510(k) premarket notification process, adhering to federal medical device regulations. The manufacturer operates from the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue9

Newest first, rows 1-9 of 9

Frequently asked questions

How many devices does Schneider-Shilley (Usa) have in the registry?

The registry currently lists 9 devices for Schneider-Shilley (Usa). Devices recorded under merged duplicate company entries are counted once.

Which registries list Schneider-Shilley (Usa)'s devices?

Among its 9 most recently registered devices, Schneider-Shilley (Usa) has devices listed in FDA 510(k) (9 devices).

What risk classes do Schneider-Shilley (Usa)'s devices fall under?

Among its 9 most recently registered devices, the classes recorded for Schneider-Shilley (Usa)'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Schneider-Shilley (Usa) in the registry?

The most recently registered devices listed for Schneider-Shilley (Usa) include MODIFIED SCHNEIDER SHILEY INFLATION SYRINGES, MODIFIED SCHNEIDER-SHILEY PRESSURE MANOMETER, SOFTRAC-PTA(TM) PERIPHERAL DILATATION CATHETER and MODIFIED OCCLUDER/FLUSHING CATHETER STOPCOCK.

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