CONTEX, INCORPORATED

FDA Device Registration & Listing · SHERMAN OAKS, CA, US · Registration 2031102

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
2031102
FEI Number
2017777
Entity Name
CONTEX, INCORPORATED
City/State/Country
SHERMAN OAKS, CA, US
Establishment Address
4505 VAN NUYS BLVD., SHERMAN OAKS, CA 91403, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Contex, Incorporated (Owner Number: 9012202)
Owner / Operator Contact Address
4505 VAN NUYS BLVD., --, Sherman Oaks, CA 91403, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Contex OK Lens Contex OK Lens Contex OK Lens

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQD Lens, Contact (Other Material) - Daily Ophthalmic Class 2 886.5916 2014-01-20
MUW Lens, Contact (Orthokeratology) Ophthalmic Class 2 886.5916 2014-01-20
NUU Lens, Contact, Orthokeratology, Overnight Ophthalmic Class 3 886.5916 2014-01-20
MWL Lens, Contact (Rigid Gas Permeable), Extended Wear Ophthalmic Class 3 886.5916 2014-01-20
MUW Lens, Contact (Orthokeratology) Ophthalmic Class 2 886.5916 2014-01-20

Official Correspondent

Steven Ernst

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Contex, Incorporated
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 2031102. Last updated year: 2026. Please use registration number 2031102 when referencing this establishment in official correspondence.
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