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Luxin Optical

⚠️ Moderate Risk

FEI: 3007475580 • Shanghai • CHINA

FEI

FEI Number

3007475580

📍

Location

Shanghai

🇨🇳

Country

CHINA
🏢

Address

1001-1007 S Pudong, , Shanghai, , China

Moderate Risk

FDA Import Risk Assessment

31.6
LowModerateHighCritical

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

Statistics

5
Total Refusals
3
Unique Violations
6/20/2016
Latest Refusal
12/19/2013
Earliest Refusal

Score Breakdown

Violation Severity
52.5×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
20.0×10%
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

2354×

NOT IMPACT

The article appears to not have impact-resistant lenses in accordance with 21 CFR 801.410.

3412×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

4762×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

Refusal History

DateProductViolationsDivision
6/20/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
476NO REGISTR
Florida District Office (FLA-DO)
6/20/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
476NO REGISTR
Florida District Office (FLA-DO)
4/21/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
341REGISTERED
Division of Southeast Imports (DSEI)
6/17/2015
86HQZFRAME, SPECTACLE
341REGISTERED
New York District Office (NYK-DO)
12/19/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Luxin Optical's FDA import refusal history?

Luxin Optical (FEI: 3007475580) has 5 FDA import refusal record(s) in our database, spanning from 12/19/2013 to 6/20/2016.

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. Luxin Optical's FEI number is 3007475580.

What types of violations has Luxin Optical received?

Luxin Optical 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 Luxin Optical come from?

All FDA import refusal data for Luxin Optical 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.