BERING LIMITED

FDA Device Registration & Listing · London London, City of, GB · Registration 3034205378

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
3034205378
FEI Number
3034205378
Entity Name
BERING LIMITED
City/State/Country
London London, City of, GB
Establishment Address
54 Portland Plance, London London, City of W1B1DY, GB
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Bering Limited (Owner Number: 10092078)
Owner / Operator Contact Address
54 Portland Plance, London, GB-LND W1B1DY, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

BraveCX

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QFM Radiological Computer-Assisted Prioritization Software For Lesions Radiology Class 2 892.2080 2024-12-02

Official Correspondent

Ignat Drozdov

US Agent Details

Stephan Toupin Business: Dawa Medical LLC Email: stoupin@dawamedical.com Phone: (786) 7311159

Related Public Records

Same Entity

Bering 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
K190362 Zebra Medical Vision, Ltd. HealthPNX 2019-05-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3034205378. Last updated year: 2026. Please use registration number 3034205378 when referencing this establishment in official correspondence.
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