Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007808978

FEI Number

3007808978

Entity Name

Veracyte, Inc.

City/State/Country

S San Fran, CA, US

Establishment Address

6000 Shoreline Ct Ste 300, S San Fran, CA 94080, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Veracyte, Inc. (Owner Number: 10035252)

Owner / Operator Contact Address

6000 Shoreline Court, Suite 300, South San Francisco, CA 94080, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Veracyte FFPE RNA Extraction Kit

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JJH	Clinical Sample Concentrator	Clinical Chemistry	Class 1	862.2310	2023-08-11

Official Correspondent

Peter Trinder

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Veracyte, Inc.

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007808978. Last updated year: 2026. Please use registration number 3007808978 when referencing this establishment in official correspondence.