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URBAN LAYER

⚠️ Moderate Risk

FEI: 3024467522 • Seongdong, Seoul • SOUTH KOREA

FEI

FEI Number

3024467522

📍

Location

Seongdong, Seoul

🇰🇷
🏢

Address

Seongsu Stn. Skv1tower, 25 Yeonmujang5ga-Gil, Seongdong, Seoul, South Korea

Moderate Risk

FDA Import Risk Assessment

45.8
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

9
Total Refusals
3
Unique Violations
12/19/2022
Latest Refusal
11/25/2022
Earliest Refusal

Score Breakdown

Violation Severity
52.0×40%
Refusal Volume
37.0×30%
Recency
24.5×20%
Frequency
90.0×10%
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

1189×

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).

32809×

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.

5082×

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
12/19/2022
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
11/29/2022
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
11/29/2022
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
11/25/2022
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
11/25/2022
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
11/25/2022
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
11/25/2022
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
11/25/2022
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
11/25/2022
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is URBAN LAYER's FDA import refusal history?

URBAN LAYER (FEI: 3024467522) has 9 FDA import refusal record(s) in our database, spanning from 11/25/2022 to 12/19/2022.

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. URBAN LAYER's FEI number is 3024467522.

What types of violations has URBAN LAYER received?

URBAN LAYER has been cited for 3 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 URBAN LAYER come from?

All FDA import refusal data for URBAN LAYER 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.