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evonos GmbH & Co. KG

GermanyFDA 510(k) applicant, unverified FDA FEI 3010726901

Devices
1,481
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

Catalogue1,481

Newest first, rows 1-50 of 1,481

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Showing 1-50 of 1,481

Company details

FDA FEI number
3010726901
Address
Stockacher Strasse 134, Tuttlingen Baden-Wurttemberg
Website
www.evonos.de
Email
[email protected](from company website)
Phone
+49 74 61 96 57 74 0(from company website)

From the company website

Read 18 Oct 2026

evonos develops, produces and distributes instruments, implants, equipment and system solutions for neurosurgery – based on work comfort.

Translated from the manufacturer's own website. Source

Frequently asked questions

How many devices does evonos GmbH & Co. KG have in the registry?

The registry currently lists 1481 devices for evonos GmbH & Co. KG. Devices recorded under merged duplicate company entries are counted once.

Which registries list evonos GmbH & Co. KG's devices?

Among its 50 most recently registered devices, evonos GmbH & Co. KG has devices listed in FDA GUDID (50 devices).

What risk classes do evonos GmbH & Co. KG's devices fall under?

Among its 50 most recently registered devices, the classes recorded for evonos GmbH & Co. KG's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from evonos GmbH & Co. KG in the registry?

The most recently registered devices listed for evonos GmbH & Co. KG include evonos WT119400, evonos WT000801, evonos WT524820 and evonos WT000803.

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