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Trend Scientific, Inc.

United StatesFDA applicant, unverified

Devices
6

What Trend Scientific, Inc. makes

Trend Scientific, Inc. manufactures diagnostic test systems for detecting parasitic infections, including Giardia, Cryptosporidium, and Entamoeba histolytica. Their products include direct detection kits for stool samples, serological ELISA test systems for amebiasis, and quality control slides for parasitology testing. These tests are designed for laboratory use to identify pathogens in clinical specimens.

The company’s portfolio includes devices classified as Class I and Class II under FDA regulations, with submissions recorded in the 510(k) clearance pathway. Products are intended for use in the United States, where regulatory compliance is required for diagnostic test systems. No additional registries or international listings are specified.

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

Catalogue6

Newest first, rows 1-6 of 6

Frequently asked questions

How many devices does Trend Scientific, Inc. have in the registry?

The registry currently lists 6 devices for Trend Scientific, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Trend Scientific, Inc.'s devices?

Among its 6 most recently registered devices, Trend Scientific, Inc. has devices listed in FDA 510(k) (6 devices).

What risk classes do Trend Scientific, Inc.'s devices fall under?

Among its 6 most recently registered devices, the classes recorded for Trend Scientific, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Trend Scientific, Inc. in the registry?

The most recently registered devices listed for Trend Scientific, Inc. include TREND GIARDIA DIRECT DETECTION RS TEST SYSTEM, FEKAL CON-TRATE SYSTEM, TREND GIARDIA LAMBLIA DIRECT DETECTION SYSTEM (MODIFIED KIT) and TREND AMEBIASIS (E.HISTOLYTICA) SEROLOGICAL ELISA TEST SYSTEM.

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