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Dr. Ing. P. Osypka, GmbH

Country not established

Devices
3

What Dr. Ing. P. Osypka, GmbH makes

Dr. Ing. P. Osypka, GmbH manufactures pacemaker leads, including models FF..D, FX..D, SZ, and RZ, which are used to connect pacemakers to the heart for electrical stimulation.

These devices are classified as Class III medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.

AI-generated from registry data, 27 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

Frequently asked questions

How many devices does Dr. Ing. P. Osypka, GmbH have in the registry?

The registry currently lists 3 devices for Dr. Ing. P. Osypka, GmbH. Devices recorded under merged duplicate company entries are counted once.

Which registries list Dr. Ing. P. Osypka, GmbH's devices?

Among its 3 most recently registered devices, Dr. Ing. P. Osypka, GmbH has devices listed in FDA 510(k) (3 devices).

What risk classes do Dr. Ing. P. Osypka, GmbH's devices fall under?

Among its 3 most recently registered devices, the classes recorded for Dr. Ing. P. Osypka, GmbH's devices are Class III. Each device page shows its own class and authorisation.

What are the newest devices from Dr. Ing. P. Osypka, GmbH in the registry?

The most recently registered devices listed for Dr. Ing. P. Osypka, GmbH include MODEL FF..D & FX..D PACEMAKER LEADS, MODEL SZ PACEMAKER LEAD-VARIOUS and MODEL RZ PACEMAKER LEAD VARIOUS.

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