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Dutchland Laboratories, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
75

What Dutchland Laboratories, Inc. makes

Dutchland Laboratories, Inc. manufactures laboratory reagents and culture media, including MINIMUM ESSENTIAL MEDIUM EAGLE W/EARLE, BABY CHICK BLOOD IN ALSEVER'S, MEM NON-ESSENTIAL AMINO ACIDS, EMEM POWERED MEDIUM, HEMOLYSIN, E-BME POWDERED MEDIUM, PENICILLIN-STREPTOMYCIN MIXTURE, HAMS F-12 POWDERED MEDIUM, FISCHER'S POWDERED MEDIUM, and RABBIT BLOOD IN ALSEVER'S, CITR., DEFIBR.

The company's products are Class I devices listed in the FDA 510(k) registry, and Dutchland Laboratories, Inc. is based in the US.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue75

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Frequently asked questions

How many devices does Dutchland Laboratories, Inc. have in the registry?

The registry currently lists 75 devices for Dutchland Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Dutchland Laboratories, Inc.'s devices?

Among its 50 most recently registered devices, Dutchland Laboratories, Inc. has devices listed in FDA 510(k) (50 devices).

What risk classes do Dutchland Laboratories, Inc.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for Dutchland Laboratories, Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Dutchland Laboratories, Inc. in the registry?

The most recently registered devices listed for Dutchland Laboratories, Inc. include MINIMUM ESSENTIAL MEDIUM EAGLE W/EARLE, BABY CHICK BLOOD IN ALSEVER'S, PARA 1 SENDAI HEMAGGLUTININ and ADULT CHICKEN BLOOD IN ALSEVER'S, C., D..

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