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REVVITY SINGAPORE PTE. LTD.

FDA registration: United States Last updated 30 May 2026 Part of Revvity Singapore Pte Ltd

Devices
14
Registries
GUDID
FDA recalls
0

Catalogue14

What REVVITY SINGAPORE PTE. LTD. makes

Revvity Singapore Pte. Ltd. manufactures in vitro diagnostic (IVD) equipment, including radioimmunoassay analysers and atomic absorption spectrophotometers. Their product line features the WIZARD² Gamma Counter for automated or semi‑automated radioimmunoassay testing and the PinAAcle900 Atomic Absorption Spectrometer for semi‑automated elemental analysis.

All of these devices are classified as Class I medical devices and are listed in the FDA UDI registry. The company is based 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

How many devices does REVVITY SINGAPORE PTE. LTD. have in the registry?

The registry currently lists 14 devices for REVVITY SINGAPORE PTE. LTD.. Devices recorded under merged duplicate company entries are counted once.

Which registries list REVVITY SINGAPORE PTE. LTD.'s devices?

Among its 14 most recently registered devices, REVVITY SINGAPORE PTE. LTD. has devices listed in FDA GUDID (14 devices).

What risk classes do REVVITY SINGAPORE PTE. LTD.'s devices fall under?

Among its 14 most recently registered devices, the classes recorded for REVVITY SINGAPORE PTE. LTD.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from REVVITY SINGAPORE PTE. LTD. in the registry?

The most recently registered devices listed for REVVITY SINGAPORE PTE. LTD. include WIZARD² Gamma Counter 2470-0010, WIZARD² Gamma Counter 2470-0100, PinAAcle900 Atomic Absorption Spectrometer N3160082 and WIZARD² Gamma Counter 3470-0150.

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

Information

FDA registration
United States(from the FDA device records)
DUNS number
894632777