Kneu Health Limited

FDA Device Registration & Listing · London London, City of, GB · Registration 3032027298

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
3032027298
FEI Number
3032027298
Entity Name
Kneu Health Limited
City/State/Country
London London, City of, GB
Establishment Address
6th Floor, 2 Kingdom Street, London London, City of W2 6BD, GB
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Kneu Health Ltd (Owner Number: 10091292)
Owner / Operator Contact Address
Blackwell House, Guildhall Yard, London, GB-LND EC2V 5AE, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Kneu Platform Kneu Platform Kneu Platform

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PTY Computerized Cognitive Assessment Aid, Exempt Neurology Class 2 882.1470 2024-08-13
NXQ Reminder, Medication Physical Medicine Class 1 890.5050 2024-08-13
GYD Transducer, Tremor Neurology Class 2 882.1950 2025-06-19

Official Correspondent

Alessia Nannetti

US Agent Details

Edwin Lindsay Business: RAF Solutions Email: edwin@rafsolutions.net Phone: (305) 9607262

Related Public Records

Same Entity

Kneu Health Ltd
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Similar Registrations

Registration Number Establishment Name Location
3043617526 AD SCIENTIAM Paris Ile-de-France, FR
3033273494 NEUROTONE AI, INC Gainesville, FL, US
3026751369 NEUROWYZR PTE LTD. Singapore Central Singapore, SG
3035679498 NEOTIV GMBH Magdeburg Saxony-Anhalt, DE
3014129043 BRAINCHECK, INC. Austin, TX, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3032027298. Last updated year: 2026. Please use registration number 3032027298 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.