KYS Vision, Inc.

FDA Device Registration & Listing · Elko, NV, US · Registration 3016965632

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
3016965632
FEI Number
3016965632
Entity Name
KYS Vision, Inc.
City/State/Country
Elko, NV, US
Establishment Address
442 Court Street, Elko, NV 89801, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
KYS Vision, Inc. (Owner Number: 10075167)
Owner / Operator Contact Address
442 Court Street, Elko, NV 89801, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Macustat Accustat Peristat

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HOQ Grid, Amsler Ophthalmic Class 1 886.1330 2020-11-13
QTO Digital Visual Acuity Test Ophthalmic Class 1 886.1150 2022-09-29
HPT Perimeter, Automatic, Ac-Powered Ophthalmic Class 1 886.1605 2025-11-14

Official Correspondent

Gary Mocnik

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

KYS 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 3016965632. Last updated year: 2026. Please use registration number 3016965632 when referencing this establishment in official correspondence.
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