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Vision Science Co., Ltd.

⚠️ High Risk

FEI: 3006946962 • Dong, Daegu • SOUTH KOREA

FEI

FEI Number

3006946962

📍

Location

Dong, Daegu

🇰🇷
🏢

Address

37-38 Maeyeoro1-Gil, , Dong, Daegu, South Korea

High Risk

FDA Import Risk Assessment

53.2
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

6
Total Refusals
5
Unique Violations
12/18/2025
Latest Refusal
11/19/2019
Earliest Refusal

Score Breakdown

Violation Severity
57.7×40%
Refusal Volume
31.3×30%
Recency
98.7×20%
Frequency
9.9×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

32805×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

1184×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

2372×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

24801×

RXPERSONAL

The article appears to be a device which requires a prescription from your doctor.

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
12/18/2025
86LPLLENSES, SOFT CONTACT, DAILY WEAR
237NO PMA
Division of Northeast Imports (DNEI)
12/3/2025
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
12/27/2023
86HQDLENS, CONTACT (OTHER MATERIAL) - DAILY
118NOT LISTED
237NO PMA
3280FRNMFGREG
Division of Southeast Imports (DSEI)
11/25/2022
86LPLLENSES, SOFT CONTACT, DAILY WEAR
3280FRNMFGREG
Division of Southeast Imports (DSEI)
11/21/2019
86LPMLENSES, SOFT CONTACT, EXTENDED WEAR
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
11/19/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
2480RXPERSONAL
3280FRNMFGREG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Vision Science Co., Ltd.'s FDA import refusal history?

Vision Science Co., Ltd. (FEI: 3006946962) has 6 FDA import refusal record(s) in our database, spanning from 11/19/2019 to 12/18/2025.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Vision Science Co., Ltd.'s FEI number is 3006946962.

What types of violations has Vision Science Co., Ltd. received?

Vision Science Co., Ltd. has been cited for 5 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about Vision Science Co., Ltd. come from?

All FDA import refusal data for Vision Science Co., Ltd. is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.