Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011422483

FEI Number

3011422483

Entity Name

VMAX VISION INC.

City/State/Country

Longwood, FL, US

Establishment Address

2170 W State Road 434 Ste 380, Longwood, FL 32779, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Vmax Vision Inc. (Owner Number: 10048615)

Owner / Operator Contact Address

2600 Maitland Center Parkway, Suite 250, Maitland, FL 32751, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

PSF Integro PSF Refractor Perfectus VASR

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HKN	Refractor, Manual, Non-Powered, Including Phoropter	Ophthalmic	Class 1	886.1770	2015-02-02
NCF	Aberrometer, Ophthalmic	Ophthalmic	Class 1	886.1760	2015-04-06

Official Correspondent

Shui Lai

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Vmax Vision Inc.

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011422483. Last updated year: 2026. Please use registration number 3011422483 when referencing this establishment in official correspondence.