CUBITTS KX LTD

FDA Device Registration & Listing · London England, GB · Registration 3012724515

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
3012724515
FEI Number
3012724515
Entity Name
CUBITTS KX LTD
City/State/Country
London England, GB
Establishment Address
55-61 Brewery Road, London England N7 9QH, GB
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Cubitts KX LTD (Owner Number: 10054746)
Owner / Operator Contact Address
55-61 Brewery Road, London, GB-ENG N79QH, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Cubitts Cubitts Cubitts Cubitts

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NJH Lens, Spectacle (Prescription), For Reading Discomfort Ophthalmic Class 1 886.5844 2024-04-03
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2022-12-01
HQY Sunglasses (Non-Prescription Including Photosensitive) Ophthalmic Class 1 886.5850 2017-04-21
HKK Telescope, Spectacle, Low-Vision Ophthalmic Class 1 886.5870 2024-04-03

Official Correspondent

Katie Dolby

US Agent Details

Vanessa Lewis Business: Cubitts Email: vanessa.lewis@cubitts.com Phone: (833) 3572082

Related Public Records

Same Entity

Cubitts KX LTD
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
K910951 United Optical, Spa OPTHLAMIC FRAMES 1991-05-06
K940726 Jay-Y Enterprises Co., Inc. NONE-GENERIC 1994-04-11
K934837 Simon Marketing, Inc. SUNGLASSES 1993-12-08
K852902 Yours Enterprise Co., Ltd. METALLIC SUNGLASSES 1985-08-12
K970895 Custom Optical Frames, Inc. CUSTOM OPTICAL SUNGLASS FRAMES 1997-05-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012724515. Last updated year: 2026. Please use registration number 3012724515 when referencing this establishment in official correspondence.
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