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Nolan Biological Laboratories, Inc.

United StatesFDA applicant, unverified

Devices
5

What Nolan Biological Laboratories, Inc. makes

Nolan Biological Laboratories, Inc. produces serodiagnostic reagents for detecting fungal infections, including Aspergillus, Candida, and Histoplasma capsulatum. Their portfolio includes immunodiffusion and serological reagents designed for laboratory identification and confirmation of these pathogens.

The company’s products are regulated under FDA’s Class I and Class II device classifications, with some cleared via the 510(k) pathway. These reagents are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue5

Newest first, rows 1-5 of 5

Frequently asked questions

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

The registry currently lists 5 devices for Nolan Biological Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Nolan Biological Laboratories, Inc.'s devices?

Among its 5 most recently registered devices, Nolan Biological Laboratories, Inc. has devices listed in FDA 510(k) (5 devices).

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

Among its 5 most recently registered devices, the classes recorded for Nolan Biological Laboratories, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Nolan Biological Laboratories, Inc. include REAGENTS FOR SERODIAGNOSIS OF ASPERGILL, REAGENTS FOR SERODIAGNOSIS OF CANDIDOSIS, IMMUNODIFFUSION REAGENTS/SEROLOGICAL and IMMUNODIFFUSSION REAGENTS/SEROLOGICAL.

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