FREEDOM OPHTHALMIC PVT LTD

FDA Device Registration & Listing · TAMIL NADU, IN · Registration 3008641313

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
3008641313
FEI Number
3008641313
Entity Name
FREEDOM OPHTHALMIC PVT LTD
City/State/Country
TAMIL NADU, IN
Establishment Address
PLOT 31 PHASE I, HOSUR DT KRISHNAGIRI, TAMIL NADU 635 126, IN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
U.S. IOL, INC. (Owner Number: 1037089)
Owner / Operator Contact Address
2500 SANDERSVILLE RD., --, Lexington, KY 40511, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Hydrophilic Acrylic IOLs 860UV and 867UV

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQL Intraocular Lens Ophthalmic Class 3 886.3600 2021-12-20

Official Correspondent

No official correspondent registered.

US Agent Details

DHAVAL SHUKLA Business: USIOL, INC. Email: INFO@usiol.com Phone: (859) 2594925

Related Public Records

Same Entity

U.S. IOL, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
1037089 U.S. IOL, INC. LEXINGTON, KY, US

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0275-2012 Abbott Medical Optics Inc (AMO) 3
Sensar Foldable IOL with OptiEdge. Model number AR40e, 6.0 Diopter. The Sensar Foldable IOLs with OptiEdge Design are ultraviolet-absorbing posterior chamber intraocular lenses and are indicated for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens are intended to be placed in a capsular bag.
Z-0276-2012 Abbott Medical Optics Inc (AMO) 3
Sensar Foldable IOL with OptiEdge. Model number AR40e 21.5 Diopter. The Sensar Foldable IOLs with OptiEdge Design are ultraviolet-absorbing posterior chamber intraocular lenses and are indicated for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens are intended to be placed in a capsular bag.
Z-0605-2010 Abbott Medical Optics Inc (AMO) 3
AMO Tecnis 1-Piece Intraocular Lens (Model ZCB00)
Z-0929-2013 Abbott Medical Optics Inc (AMO) 3
AMO Sensar Intraocular Lenses (IOLs), Model AR40e, Sensar Foldable IOL with OptiEdge Product Usage: These are ultraviolet-absorbing posterior chamber intraocular lenses for use after cataract extraction.
Z-2287-2020 Alcon Research LLC Aspex Facility 3
Acrysof, IQ IOL w/UltraSert System, AcrySof IQ ASPHERIC IOL, 20.5 D, SP ACRYLIC FOLDABLE LENS, w/UltraSert DELIVERY SYSTEM, UV w/BLUE LIGHT FILTER. 13.0mm. LENGTH, 6.0mm ANTERIOR ASYMMETRIC BICONVEX OPTIC, PLANAR HAPTICS.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008641313. Last updated year: 2026. Please use registration number 3008641313 when referencing this establishment in official correspondence.
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