Vision Rx Lab Pvt. Ltd.

FDA Device Registration & Listing · Gurgaon Haryana, IN · Registration 3008164710

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
3008164710
FEI Number
3008164710
Entity Name
Vision Rx Lab Pvt. Ltd.
City/State/Country
Gurgaon Haryana, IN
Establishment Address
A-15, Infocity,, Sector 34, Gurgaon Haryana 122001, IN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Remanufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Vision Rx Lab Pvt. Ltd. (Owner Number: 9035999)
Owner / Operator Contact Address
P-4, Kasba Industrial Estate, Phase I, Kolkata, West Bengal, IN-WB 700 107, IN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Rx Eyeglasses Sunglass Frame - Non Rx Prescription Optical Frame Vision Rx Lab, Nova Brands, Prescription Ophthalmic Lenses

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HOI Spectacle, Magnifying Ophthalmic Class 1 886.5840 2010-03-29
HQY Sunglasses (Non-Prescription Including Photosensitive) Ophthalmic Class 1 886.5850 2010-03-29
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2010-03-29
HQG Lens, Spectacle, Non-Custom (Prescription) Ophthalmic Class 1 886.5844 1998-12-28
NJH Lens, Spectacle (Prescription), For Reading Discomfort Ophthalmic Class 1 886.5844 2010-03-29

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Vision Rx Lab Pvt. 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
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
K853921 Winsburn Company , Ltd. ALL KINDS OF SUNGLASSES 1985-10-15

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008164710. Last updated year: 2026. Please use registration number 3008164710 when referencing this establishment in official correspondence.
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