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voss medical products

Country not established FDA establishment FEI 1643116

Devices
5
Registrations
FDA
FDA recalls
0

What voss medical products makes

Voss Medical Products makes disposable coronary bypass flushing cannulas, bypass leg positioners, graft markers, vein clamps, and prone positioners.

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

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue5

Newest first, rows 1-5 of 5

Company details

FDA FEI number
1643116
Address
4235 centergate, San Antonio, TX, 78217

Frequently asked questions

How many devices does voss medical products have in the registry?

The registry currently lists 5 devices for voss medical products. Devices recorded under merged duplicate company entries are counted once.

Which registries list voss medical products's devices?

Among its 5 most recently registered devices, voss medical products has devices listed in FDA 510(k) (5 devices).

What risk classes do voss medical products's devices fall under?

Among its 5 most recently registered devices, the classes recorded for voss medical products's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from voss medical products in the registry?

The most recently registered devices listed for voss medical products include VOSS DISPOSABLE CORONARY BYPASS FLUSHING CANNULA, BYPASS LEG POSITIONER, VOSS GRAFT MARKER and VOSS VEIN CLAMP.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.