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Contact My Eyes

⚠️ Moderate Risk

FEI: 3011328508 • Noida, Uttar Pradesh • INDIA

FEI

FEI Number

3011328508

📍

Location

Noida, Uttar Pradesh

🇮🇳

Country

INDIA
🏢

Address

J-35 Sec 18, First Floor, Noida, Uttar Pradesh, India

Moderate Risk

FDA Import Risk Assessment

29.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
4
Unique Violations
10/13/2015
Latest Refusal
10/13/2015
Earliest Refusal

Score Breakdown

Violation Severity
62.5×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

1181×

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).

2371×

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).

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
10/13/2015
86MWLLENS, CONTACT (RIGID GAS PERMEABLE) - EXTENDED WEAR
118NOT LISTED
237NO PMA
3280FRNMFGREG
508NO 510(K)
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Contact My Eyes's FDA import refusal history?

Contact My Eyes (FEI: 3011328508) has 1 FDA import refusal record(s) in our database, spanning from 10/13/2015 to 10/13/2015.

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. Contact My Eyes's FEI number is 3011328508.

What types of violations has Contact My Eyes received?

Contact My Eyes 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 Contact My Eyes come from?

All FDA import refusal data for Contact My Eyes 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.