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Dr. Bruno Lange GmbH

Country not established

Devices
5

What Dr. Bruno Lange GmbH makes

Dr. Bruno Lange GmbH manufactures photometers, including the LP 1, LP 3, LP 6, and LP 300 models, as well as flame photometers.

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

AI-generated from registry data, 23 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue5

Newest first, rows 1-5 of 5

  • Photometer LP 3 Ref K801563

    Class I
    Active 510(k) 510(k) I
  • Photometer LP 300 Ref K832531

    Class I
    Active 510(k) 510(k) I
  • Photometer LP 6 Ref K801562

    Class I
    Active 510(k) 510(k) I
  • Flame Photometers Ref K834226

    Class I
    Active 510(k) 510(k) I
  • Photometer LP 1 Ref K801564

    Class I
    Active 510(k) 510(k) I

Frequently asked questions

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

The registry currently lists 5 devices for Dr. Bruno Lange GmbH. Devices recorded under merged duplicate company entries are counted once.

Which registries list Dr. Bruno Lange GmbH's devices?

Among its 5 most recently registered devices, Dr. Bruno Lange GmbH has devices listed in FDA 510(k) (5 devices).

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

Among its 5 most recently registered devices, the classes recorded for Dr. Bruno Lange GmbH's devices are Class I. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Dr. Bruno Lange GmbH include PHOTOMETER LP 3, PHOTOMETER LP 300, PHOTOMETER LP 6 and FLAME PHOTOMETERS.

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