Healthcare Outcomes Performance Company Ltd

FDA Device Registration & Listing · London London, City of, GB · Registration 3023744170

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
3023744170
FEI Number
3023744170
Entity Name
Healthcare Outcomes Performance Company Ltd
City/State/Country
London London, City of, GB
Establishment Address
Healthcare Outcomes Performance Company Ltd dba HOPCo, hopper, myrecovery & msk.ai, Hale House (42 Portland Place), London London, City of W1B 1NB, GB
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Healthcare Outcomes Performance Company Ltd (Owner Number: 10085719)
Owner / Operator Contact Address
Healthcare Outcomes Performance Company Ltd, Hale House (42 Portland Place), London, GB-LND W1B 1NB, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

myrecovery, myrecovery Patient Engagement & Outcomes Solution, myrecovery by HOPCo, msk.ai, msk.ai Deep Vision myrecovery, myrecovery by HOPCo, hopper OS, hopper by HOPCo, hopper OS by HOPCo, msk.ai

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KQX Goniometer, Ac-Powered Orthopedic Class 1 888.1500 2022-07-26
OUG Medical Device Data System General Hospital Class 1 880.6310 2022-07-26

Official Correspondent

Axel Sylvan

US Agent Details

Marc Jacofsky Email: marc.jacofsky@hopco.com Phone: (623) 2418618

Related Public Records

Same Entity

Healthcare Outcomes Performance Company Ltd
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 3023744170. Last updated year: 2026. Please use registration number 3023744170 when referencing this establishment in official correspondence.
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