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CooperVision CL KFT

⚠️ High Risk

FEI: 3009108089 • Gyal, Pest • HUNGARY

FEI

FEI Number

3009108089

📍

Location

Gyal, Pest

🇭🇺

Country

HUNGARY
🏢

Address

Gorcsev Ivan Street 7 Bldg/C, , Gyal, Pest, Hungary

High Risk

FDA Import Risk Assessment

62.4
LowModerateHighCritical

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

Statistics

16
Total Refusals
4
Unique Violations
11/28/2025
Latest Refusal
7/30/2019
Earliest Refusal

Score Breakdown

Violation Severity
66.7×40%
Refusal Volume
45.6×30%
Recency
97.6×20%
Frequency
25.3×10%
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

248014×

RXPERSONAL

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

1182×

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).

32801×

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.

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
11/28/2025
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
508NO 510(K)
Division of Southeast Imports (DSEI)
8/13/2021
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
6/18/2020
86MVNLENS, CONTACT (DISPOSABLE)
2480RXPERSONAL
Division of Northern Border Imports (DNBI)
7/30/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
2480RXPERSONAL
Division of Southeast Imports (DSEI)
7/30/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
2480RXPERSONAL
Division of Southeast Imports (DSEI)
7/30/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
2480RXPERSONAL
Division of Southeast Imports (DSEI)
7/30/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
2480RXPERSONAL
Division of Southeast Imports (DSEI)
7/30/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
2480RXPERSONAL
Division of Southeast Imports (DSEI)
7/30/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
2480RXPERSONAL
Division of Southeast Imports (DSEI)
7/30/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
2480RXPERSONAL
Division of Southeast Imports (DSEI)
7/30/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
2480RXPERSONAL
Division of Southeast Imports (DSEI)
7/30/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
2480RXPERSONAL
Division of Southeast Imports (DSEI)
7/30/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
2480RXPERSONAL
Division of Southeast Imports (DSEI)
7/30/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
2480RXPERSONAL
Division of Southeast Imports (DSEI)
7/30/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
2480RXPERSONAL
Division of Southeast Imports (DSEI)
7/30/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
2480RXPERSONAL
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is CooperVision CL KFT's FDA import refusal history?

CooperVision CL KFT (FEI: 3009108089) has 16 FDA import refusal record(s) in our database, spanning from 7/30/2019 to 11/28/2025.

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. CooperVision CL KFT's FEI number is 3009108089.

What types of violations has CooperVision CL KFT received?

CooperVision CL KFT has been cited for 4 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 CooperVision CL KFT come from?

All FDA import refusal data for CooperVision CL KFT 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.