Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3032324401

FEI Number

3032324401

Entity Name

Revvity Discovery Limited

City/State/Country

Cambrige Cambridgeshire, GB

Establishment Address

Building 8100, Cambridge Research Park, Cambrige Cambridgeshire CB25 9TL, GB

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Revvity, Inc. (Owner Number: 9912035)

Owner / Operator Contact Address

77 4th Avenue, Waltham, MA 02451, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OHQ	Multi-Analyte Controls Unassayed	Clinical Chemistry	Class 1	862.1660	2022-08-19

Official Correspondent

Daniel Castellanos

US Agent Details

Daniel Castellanos Business: REVVITY, INC. Email: americas.regulatory@revvity.com Phone: (408) 8235561

Related Public Records

Same Entity

Revvity, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3004049804	Revvity Singapore Pte Ltd	Singapore Central Singapore, SG
3007145015	Revvity Health Sciences, Inc.	Greenville, SC, US
3009981484	Revvity Health Sciences, Inc.	Hopkinton, MA, US
8043909	WALLAC OY	TURKU Varsinais-Suomi, FI

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2250051	ORTHO-CLINICAL DIAGNOSTICS, INC.	RARITAN, NJ, US
3021090658	Ortho-Clinical Diagnostics, Inc.	Carlsbad, CA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3032324401. Last updated year: 2026. Please use registration number 3032324401 when referencing this establishment in official correspondence.