Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011503801

FEI Number

3011503801

Entity Name

Plexus Optix, Inc.

City/State/Country

Rancho Cordova, CA, US

Establishment Address

11135 Trade Center Dr Ste 130, Rancho Cordova, CA 95670, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Plexus Optix, Inc. (Owner Number: 10049041)

Owner / Operator Contact Address

11135 Trade Center Drive, Suite 130, Rancho Cordova, CA 95670, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Plexus

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	2015-04-06

Official Correspondent

John Humphreys

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Plexus Optix, Inc.

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

View Entity Profile →

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3007675955	Carl Zeiss Vision Canada, Inc.	Toronto Ontario, CA
1000428458	GKB OPHTHALMICS LIMITED - UNIT II	North Goa Goa, IN
3038136215	MEIVISION (VIETNAM) CO., LTD	Ho Chi Minh City, VN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011503801. Last updated year: 2026. Please use registration number 3011503801 when referencing this establishment in official correspondence.