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Molecular Devices Corp.

United StatesFDA applicant, unverified

Devices
4

What Molecular Devices Corp. makes

Molecular Devices Corp. manufactures microplate readers designed for kinetic and endpoint absorbance measurements in laboratory settings. These instruments include the UVMAX, THERMOMAX, VMAX, and EMAX series, which support high-throughput assays in research and diagnostics. The devices are optimized for multi-well plate analysis across various wavelengths, enabling automated data collection for biochemical and cell-based experiments.

The company’s microplate readers are classified as Class I medical devices under FDA regulations and are recorded in the 510(k) clearance database. These instruments are intended for use in non-clinical and research environments, adhering to standard safety and performance requirements for low-risk devices. The portfolio is listed in the U.S. regulatory system without additional third-party certification.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue4

Newest first, rows 1-4 of 4

Frequently asked questions

How many devices does Molecular Devices Corp. have in the registry?

The registry currently lists 4 devices for Molecular Devices Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Molecular Devices Corp.'s devices?

Among its 4 most recently registered devices, Molecular Devices Corp. has devices listed in FDA 510(k) (4 devices).

What risk classes do Molecular Devices Corp.'s devices fall under?

Among its 4 most recently registered devices, the classes recorded for Molecular Devices Corp.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Molecular Devices Corp. in the registry?

The most recently registered devices listed for Molecular Devices Corp. include UVMAX KINETIC MICROPLATE READER, THERMOMAX MICROPLATE READER, MODIFICATION, VMAX KINETIC MICROPLATE READER and EMAX PRECISION MICROPLATE READER.

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