Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030184056

FEI Number

3030184056

Entity Name

IMPORTADORA PRIMEX, S.A. DE C.V.

City/State/Country

Tepeji del Rio Hidalgo, MX

Establishment Address

Avenida Central #3 Lote 1 Manzana 847, Parque Industrial, Tepeji del Rio Hidalgo 42580, MX

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

Importadora Primex (Owner Number: 10089302)

Owner / Operator Contact Address

Avenida Central #3 Lote 1 Manzana 847, Parque Industrial, Tepeji del Rio, MX-HID 42580, MX

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

1879785 Hi index 1.67 Transitions Gray 1879787 Hi index Transitions Green 1879786 Hi index 1.67 Transitions Brown

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQG	Lens, Spectacle, Non-Custom (Prescription)	Ophthalmic	Class 1	886.5844	2023-11-27

Official Correspondent

Roberto Martinez Paredes

US Agent Details

Nikki Bowman Business: Costco Wholesale Corporation Email: NBowman@costco.com Phone: (425) 3138100

Related Public Records

Same Entity

Importadora Primex

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

View Entity Profile →

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1000428458	GKB OPHTHALMICS LIMITED - UNIT II	North Goa Goa, IN
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030184056. Last updated year: 2026. Please use registration number 3030184056 when referencing this establishment in official correspondence.