MOTILENT LTD

FDA Device Registration & Listing · London England, GB · Registration 3030179922

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
3030179922
FEI Number
3030179922
Entity Name
MOTILENT LTD
City/State/Country
London England, GB
Establishment Address
Beyond, Aldgate Tower - Motilent Ltd., 2 Leman Street, London England E1 8FA, GB
Establishment Type(s)
Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Motilent LTD (Owner Number: 10089117)
Owner / Operator Contact Address
Beyond, Aldgate Tower - Motilent Ltd., 2 Leman Street, London, GB-ENG E1 8FA, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Entrolytics MD

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LMD System, Digital Image Communications, Radiological Radiology Class 1 892.2020 2023-11-07

Official Correspondent

Alex Menys

US Agent Details

Emily Matorin Business: FDAbasics Email: usagent@fdabasics.com Phone: (716) 7750533

Related Public Records

Same Entity

Motilent 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 3030179922. Last updated year: 2026. Please use registration number 3030179922 when referencing this establishment in official correspondence.
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