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Dr. Fritz GmbH

Country not established

Devices
1

What Dr. Fritz GmbH makes

Dr. Fritz GmbH manufactures a modular instrument system for minimal invasive surgery.

The company's products are listed in the FDA 510(k) registry and are classified as Class II devices. Dr. Fritz GmbH is based in the US.

AI-generated from registry data, 25 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

Frequently asked questions

How many devices does Dr. Fritz GmbH have in the registry?

The registry currently lists 1 device for Dr. Fritz GmbH. Devices recorded under merged duplicate company entries are counted once.

Which registries list Dr. Fritz GmbH's devices?

Among its 1 most recently registered device, Dr. Fritz GmbH has devices listed in FDA 510(k) (1 device).

What risk classes do Dr. Fritz GmbH's devices fall under?

Among its 1 most recently registered device, the classes recorded for Dr. Fritz GmbH's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Dr. Fritz GmbH in the registry?

The most recently registered devices listed for Dr. Fritz GmbH include MODULAR INSTRUMENT SYSTEM FOR MINIMAL INVASIVE SURGERY.

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