WHITERABBIT AI INC

FDA Device Registration & Listing · Redwood City, CA, US · Registration 3017976149

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3017976149
FEI Number
3017976149
Entity Name
WHITERABBIT AI INC
City/State/Country
Redwood City, CA, US
Establishment Address
255 Shoreline Drive, Suite 428, Redwood City, CA 94065, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Whiterabbit.ai (Owner Number: 10079235)
Owner / Operator Contact Address
255 Shoreline Drive, Suite 428, Redwood City, CA 94065, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

WRDensity by Whiterabbit.ai

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QIH Automated Radiological Image Processing Software Radiology Class 2 892.2050 2020-12-22

Official Correspondent

Marguerite Thomlinson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Whiterabbit.ai
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K242270 Orthofix Srl OrthoNext Platform System 2024-12-19
K261713 FUJIFILM Healthcare Americas Corporation Synapse PACS (7.6.0) 2026-06-18
K243647 FUJIFILM Healthcare Americas Corporation Synapse PACS (7.5) 2025-06-30

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017976149. Last updated year: 2026. Please use registration number 3017976149 when referencing this establishment in official correspondence.
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