Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007085310

FEI Number

3007085310

Entity Name

20/20 Medical Systems, Inc.

City/State/Country

Crystal Lake, IL, US

Establishment Address

111 Erick Street, Unit 125, Crystal Lake, IL 60014, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

20/20 Medical Systems, Inc. (Owner Number: 10033891)

Owner / Operator Contact Address

55 Parkview Court, Crystal Lake, IL 60012, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

K2042RTP3 K2 Tables LAB-4002 K2446VTP3 K1620SL-Z K2036RTP5 K2042RTPX K2032RTPX K2032RT K2032GT K2056RTP3 K2026RTPX K2428RT UDS-101 K2042RTP4 K2-110C K2020GT UDS-201 K2036RTPX K2036RTP3 K2-220KR K2748SWRP2 K2748SWLP4 K2042RTP2 K2857DWP3 K1832RTPX HGRP-M8 K2428RTP3 CST63-LX4 K2026RT K2-230C K1832RT K2-220CN K1620SL K2036RTP1 K2433RTP1

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HRJ	Table, Instrument, Powered, Ophthalmic	Ophthalmic	Class 1	886.4855	2010-10-14

Official Correspondent

Gary Chianakas

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

20/20 Medical Systems, 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 3007085310. Last updated year: 2026. Please use registration number 3007085310 when referencing this establishment in official correspondence.