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Revvity Health Sciences, Inc - MA

United States US-MF-000023091 Last updated 21 Oct 2026

Devices
47
Registries
EUDAMEDGUDID
FDA recalls
0

Catalogue47

Authorised representatives

What Revvity Health Sciences, Inc - MA makes

The company manufactures automated liquid handling workstations, including the Fontus and JANUS G3 models, designed for precise fluid transfer and sample processing in laboratory settings. These systems are engineered to streamline workflows for tasks such as reagent dispensing, cell culture handling, and multi-step assay automation. The devices are built to integrate with laboratory information management systems (LIMS) and support high-throughput applications. They are primarily used in research, biopharmaceutical development, and clinical diagnostics environments.

The automated liquid handling workstations fall under EU Class A medical devices and are registered in the EUDAMED database. While the devices are listed in the European Union’s medical device registry, their regulatory status depends on individual market authorisations. The company is headquartered in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Revvity Health Sciences, Inc manufacture?

Revvity Health Sciences, Inc specialises in automated liquid handling workstations, such as the Fontus and JANUS G3 models. These devices are designed for precise fluid transfer and sample processing in laboratories, automating tasks like reagent dispensing, cell culture handling, and multi-step assay procedures. They are tailored for high-throughput workflows and can integrate with laboratory information management systems (LIMS), making them suitable for research, biopharmaceutical development, and clinical diagnostics.

Where is Revvity Health Sciences, Inc based?

Revvity Health Sciences, Inc is headquartered in Massachusetts, United States. The company’s location in the US reflects its focus on developing and manufacturing automated liquid handling solutions for global laboratory markets.

Are Revvity Health Sciences, Inc’s devices listed in any regulatory registries?

Yes, Revvity Health Sciences, Inc’s automated liquid handling workstations are registered in the EUDAMED database, which is the European Union’s medical device registry. This listing applies to the devices as Class A medical devices under EU regulations, though individual market authorisations determine their regulatory status in specific regions.

How are Revvity Health Sciences, Inc’s automated liquid handling workstations classified?

Revvity Health Sciences, Inc’s automated liquid handling workstations are classified as Class A medical devices in the European Union. This classification is based on their intended use—non-invasive, low-risk applications like precise fluid handling in laboratory settings—which aligns with EU regulatory criteria for minimal risk devices. Classification determines the regulatory pathway for market authorisation, but it does not imply approval or clearance.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
United States(from SRN)
Address
68, Elm Street, Hopkinton, United States
PRRC contact
Paul Caracciolo
EUDAMED SRN
US-MF-000023091