Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012304651

FEI Number

3012304651

Entity Name

Rayner Intraocular Lenses Limited

City/State/Country

Worthing West Sussex, GB

Establishment Address

The Ridley Innovation Centre, 10 Dominion Way, Worthing West Sussex BN14 8AQ, GB

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Rayner Intraocular Lenses Limited (Owner Number: 8010143)

Owner / Operator Contact Address

The Ridley Innovation Centre, 10 Dominion Way, Worthing, GB-WSX BN14 8AQ, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P060011

All Registered Proprietary Names

Model RAO600C Model RAO100C RayOne EMV Toric Model RAO200E

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MJP	Lens, Intraocular, Toric Optics	Ophthalmic	Class 3	886.3600	2007-12-12
HQL	Intraocular Lens	Ophthalmic	Class 3	886.3600	2007-12-12

Official Correspondent

No official correspondent registered.

US Agent Details

Scott Corning Business: Rayner Surgical Inc. Email: scottcorning@rayner.com Phone: (901) 4124907

Related Public Records

Same Entity

Rayner Intraocular Lenses Limited

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0028-2022	Johnson & Johnson Surgical Vision Inc	3	TECNIS Eyhance IOLs are permanent intraocular implants intended for implantation in the capsular bag. The TECNIS Simplicity Delivery System is designed as a single-use disposable preloaded modular cartridge that functions as both the primary packaging and as a sterile, disposable insertion system for delivering the IOL into the eye during cataract surgery.
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.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012304651. Last updated year: 2026. Please use registration number 3012304651 when referencing this establishment in official correspondence.