PRECISION VISION

FDA Device Registration & Listing · Woodstock, IL, US · Registration 3003846146

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
3003846146
FEI Number
3003846146
Entity Name
PRECISION VISION
City/State/Country
Woodstock, IL, US
Establishment Address
1725 Kilkenny Court, Woodstock, IL 60098, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Precision Vision (Owner Number: 10025481)
Owner / Operator Contact Address
1725 Kilkenny Court, Woodstock, IL 60098, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Jackson Cross Cylinder PV Trial Lenses Precision Vision, Inc. Cabinet, Instrument, Ac-powered, Ophthalmic Ophthalmic Trial Lens Frame Ophthalmic Trial Lens Set Jackson Cross Cylinder PV Trial Lenses PV Trial Lenses

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HPA Frame, Trial, Ophthalmic Ophthalmic Class 1 886.1415 2019-08-22
HRE Cabinet, Instrument, Ac-Powered, Ophthalmic Ophthalmic Class 1 886.1860 2014-12-22
HIT Tester, Color Vision Ophthalmic Class 1 886.1170 2008-04-17
HOX Chart, Visual Acuity Ophthalmic Class 1 886.1150 2008-04-17
HPA Frame, Trial, Ophthalmic Ophthalmic Class 1 886.1415 2019-08-22
HPC Set, Lens, Trial, Ophthalmic Ophthalmic Class 1 886.1405 2019-08-22

Official Correspondent

Ed Kopidlansky

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Precision Vision
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
K900478 Woodlyn, Inc. WOODLYN FULL APERTURE TRIAL LENS SET 1990-02-21

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003846146. Last updated year: 2026. Please use registration number 3003846146 when referencing this establishment in official correspondence.
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