Acurable Limited

FDA Device Registration & Listing · London London, City of, GB · Registration 3024891505

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
3024891505
FEI Number
3024891505
Entity Name
Acurable Limited
City/State/Country
London London, City of, GB
Establishment Address
2 Leman Street, London E1W 9US, London London, City of E1W 9US, GB
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Acurable Limited (Owner Number: 10086249)
Owner / Operator Contact Address
83 Victoria Street, London, GB-LND SW1H 0HW, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

AcuPebble SA100 AcuPebble Ox100

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MNR Ventilatory Effort Recorder Anesthesiology Class 2 868.2375 2022-10-26
MNR Ventilatory Effort Recorder Anesthesiology Class 2 868.2375 2023-10-18

Official Correspondent

Esther Rodriguez-Villegas

US Agent Details

Stephan Toupin Business: Dawa Medical LLC Email: stoupin@dawamedical.com Phone: (786) 7211159

Related Public Records

Same Entity

Acurable Limited
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
K082968 Apneicare, LLC APNEICARE CONNECTION CENTER/INTERNET ANALYSIS 2009-01-02

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0031-2022 NOX MEDICAL Keldnaholt Reykjavik Iceland 2
Nox T3s Recorder - Product Usage: intended for ambulatory recording of physiological signals during sleep.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3024891505. Last updated year: 2026. Please use registration number 3024891505 when referencing this establishment in official correspondence.
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