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Pudenz-Schulte Medical Research Corp.

United StatesFDA applicant, unverified

Devices
40

What Pudenz-Schulte Medical Research Corp. makes

Pudenz-Schulte Medical Research Corp. manufactures medical devices for cerebrospinal fluid (CSF) access, including ventricular catheters, flanged reservoirs, and subcutaneous access ports. Their portfolio also includes vascular access catheters, catheter placement kits, and dual-lumen ports for intraperitoneal and ventricular applications. Disposable subcutaneous catheter passers and specialized CSF-on/off flushing reservoirs are also part of their product line.

The company’s devices are regulated under FDA Class I and Class II classifications, with several products listed via the 510(k) pathway. These devices are intended for use in the US, where they are subject to FDA oversight. The company 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 Pudenz-Schulte Medical Research Corp. have in the registry?

The registry currently lists 40 devices for Pudenz-Schulte Medical Research Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Pudenz-Schulte Medical Research Corp.'s devices?

Among its 40 most recently registered devices, Pudenz-Schulte Medical Research Corp. has devices listed in FDA 510(k) (40 devices).

What risk classes do Pudenz-Schulte Medical Research Corp.'s devices fall under?

Among its 40 most recently registered devices, the classes recorded for Pudenz-Schulte Medical Research Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Pudenz-Schulte Medical Research Corp. in the registry?

The most recently registered devices listed for Pudenz-Schulte Medical Research Corp. include P-S MEDICAL CSF ACCESS DEV 15MM/25MM, PS MEDICAL IPI VASCULAR ACCESS CATHETER, PS MEDICAL CATHETER PLACEMENT KIT and CSF-CARDIAC/PERITONEAL CATHETER.

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