GKB HI-TECH MIDDLE EAST

FDA Device Registration & Listing · SHARJAH Ash Shariqah, AE · Registration 3009093215

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
3009093215
FEI Number
3009093215
Entity Name
GKB HI-TECH MIDDLE EAST
City/State/Country
SHARJAH Ash Shariqah, AE
Establishment Address
WAREHOUSE Q4 51, SAIFZONE, SHARJAH Ash Shariqah 122290, AE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
GKB HI-TECH MIDDLE EAST (Owner Number: 10038803)
Owner / Operator Contact Address
WAREHOUSE Q4 51, SAIFZONE, SHARJAH, AE-NOTA 122290, AE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Swiss Kodak Ophthalmic Lens Matrix Solo Asahi Lite Multicom

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 2011-11-14

Official Correspondent

Shobit Gupta

US Agent Details

Kiran Desai Business: Lensco The Lens Company Email: kiran.desai@lensco.net Phone: (973) 5460866

Related Public Records

Same Entity

GKB HI-TECH MIDDLE EAST
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 3009093215. Last updated year: 2026. Please use registration number 3009093215 when referencing this establishment in official correspondence.
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