COGENT TECHNOLOGY LIMITED

FDA Device Registration & Listing · Felixstowe Suffolk, GB · Registration 3002806730

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
3002806730
FEI Number
3002806730
Entity Name
COGENT TECHNOLOGY LIMITED
City/State/Country
Felixstowe Suffolk, GB
Establishment Address
Landguard Point Enterprise Centre, Langer Road, Felixstowe Suffolk IP11 2BF, GB
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
COGENT TECHNOLOGY LIMITED (Owner Number: 9085287)
Owner / Operator Contact Address
Langer Road, Felixstowe, GB-SFK IP11 2BF, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

VDD-AKITAJET MEEB2 ME-MDRIVE MEPUN ME-MPR ACH-SOLO MEURUTH MEURUAB

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CAF Nebulizer (Direct Patient Interface) Anesthesiology Class 2 868.5630 2017-02-10
OLV Standard Polysomnograph With Electroencephalograph Neurology Class 2 882.1400 2006-04-03
MNR Ventilatory Effort Recorder Anesthesiology Class 2 868.2375 2012-12-21
MNR Ventilatory Effort Recorder Anesthesiology Class 2 868.2375 2006-04-03
MNR Ventilatory Effort Recorder Anesthesiology Class 2 868.2375 2013-08-06
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2015-12-24
MNR Ventilatory Effort Recorder Anesthesiology Class 2 868.2375 2012-12-21

Official Correspondent

No official correspondent registered.

US Agent Details

David Milne Email: david.milne@natus.com Phone: (317) 4465267

Related Public Records

Same Entity

COGENT TECHNOLOGY 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
K163485 Adherium (Nz), Ltd. SmartTouch 2017-08-30
K781467 Travenol Laboratories, S.A. U-FLOAT VALVE 2D9023 1978-09-07
K161650 Neurotronics, Inc. Polysmith Sleep System, Model NTI7593 2017-01-19
K082968 Apneicare, LLC APNEICARE CONNECTION CENTER/INTERNET ANALYSIS 2009-01-02
K122948 Gemore Technology Co, Ltd. GEM-STIM COMBO STIMULATOR 2012-12-21

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 3002806730. Last updated year: 2026. Please use registration number 3002806730 when referencing this establishment in official correspondence.
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