GRANDEUR

FDA Device Registration & Listing · NEW DELHI 110020, IN · Registration 3002499749

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
3002499749
FEI Number
3002499749
Entity Name
GRANDEUR
City/State/Country
NEW DELHI 110020, IN
Establishment Address
F-90/27, OKHLA INDUSTRIAL AREA, PHASE-I, NEW DELHI 110020 110020, IN
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
GRANDEUR (Owner Number: 10052251)
Owner / Operator Contact Address
F-90/27, OKHLA INDUSTRIAL AREA, PHASE-I, NEW DELHI 110020, IN-DL 110020, IN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

frame trial set magnifier Spectacle goggle clip Frame Trial Eye Shield

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2016-07-06
HPC Set, Lens, Trial, Ophthalmic Ophthalmic Class 1 886.1405 2016-07-06
HJF Magnifier, Hand-Held, Low-Vision Ophthalmic Class 1 886.5540 2016-07-06
HOH Spectacle, Operating (Loupe), Ophthalmic Ophthalmic Class 1 886.4770 2016-07-06
HPB Clip, Lens, Trial, Ophthalmic Ophthalmic Class 1 886.1410 2016-07-06
HPA Frame, Trial, Ophthalmic Ophthalmic Class 1 886.1415 2016-07-06
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) Ophthalmic Class 1 886.4750 2016-07-06

Official Correspondent

SIMRAN TEJUJA

US Agent Details

ASHISH KHOSLA Email: nicktejuja@gmail.com Phone: (703) 6254700

Related Public Records

Same Entity

GRANDEUR
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
K900478 Woodlyn, Inc. WOODLYN FULL APERTURE TRIAL LENS SET 1990-02-21

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3002499749. Last updated year: 2026. Please use registration number 3002499749 when referencing this establishment in official correspondence.
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