CONTAMAC LTD.

FDA Device Registration & Listing · ESSEX UK, GB · Registration 3001190611

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
3001190611
FEI Number
3001190611
Entity Name
CONTAMAC LTD.
City/State/Country
ESSEX UK, GB
Establishment Address
CARLTON HOUSE, SHIREHILL, ESSEX UK CB11 3AU, GB
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
CONTAMAC LTD. (Owner Number: 9011725)
Owner / Operator Contact Address
SAFFRON WALDEN, Carlton House, Shire Hill, ESSEX, GB-NOTA CB11-3AU, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
P240045

All Registered Proprietary Names

Optimum Infinite SynergEyes GP Bitoric Extra Progressive Plus SynergEyes VS SynergEyes GP Progressive D SynergEyes GP II Progressive D SynergEyes GP II Bitoric Extra Progressive SynergEyes GP II SynergEyes GP II Progressive N SynergEyes VS XL QT SynergEyes GP II Bitoric EP SynergEyes GP Progressive D Plus SynergEyes VS XL Sphere SynergEyes GP Progressive N SynergEyes VS XL SynergEyes GP II Bitoric Extra EP SynergEyes GP II EP SynergEyes GP II Bitoric Extra SynergEyes GP II Progressive D Plus SynergEyes GP EP SynergEyes GP Bitoric SynergEyes GP II Bitoric Progressive SynergEyes GP SynergEyes GP Bitoric Extra SynergEyes GP Bitoric Extra Progressive SynergEyes GP Bitoric Progressive Plus SynergEyes GP Bitoric Progressive SynergEyes GP II Bitoric SynergEyes GP Front toric SynergEyes VS Sphere Optimum Dry EYE Lens Scleral Dry EYE Lens SynergEyes VS Optimum GP SynergEyes VS MF EyeFitPRO ScanFitPRO EyePrintPRO Optimum Infinite Orthokeratology Lenses II

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MUW Lens, Contact (Orthokeratology) Ophthalmic Class 2 886.5916 2020-07-21
HQD Lens, Contact (Other Material) - Daily Ophthalmic Class 2 886.5916 2020-07-21
HQD Lens, Contact (Other Material) - Daily Ophthalmic Class 2 886.5916 2018-10-24
HQD Lens, Contact (Other Material) - Daily Ophthalmic Class 2 886.5916 2018-06-26
NUU Lens, Contact, Orthokeratology, Overnight Ophthalmic Class 3 886.5916 2026-04-23

Official Correspondent

Robert McGregor

US Agent Details

Bret Andre Business: EYEREG CONSULTING INC. Email: bandre@fdapproval.com Phone: (503) 3725226

Related Public Records

Same Entity

CONTAMAC 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
K963512 Benz Research and Development Corp. BENZ B17 (KOLFOCON A) RIGID GAS PERMEABLE (HYDROPHOBIC DAILY WEAR CONTACT LENS (CLEAR AND TINTED, LATHE-CUT FROM LENS BL 1997-07-31

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3001190611. Last updated year: 2026. Please use registration number 3001190611 when referencing this establishment in official correspondence.
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