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ALCON MANAGEMENT S.A.

⚠️ Moderate Risk

FEI: 3015911840 • Vernier, Geneva • SWITZERLAND

FEI

FEI Number

3015911840

📍

Location

Vernier, Geneva

🇨🇭
🏢

Address

Chemin De Blandonnet 8, Geneva, Vernier, Geneva, Switzerland

Moderate Risk

FDA Import Risk Assessment

48.5
LowModerateHighCritical

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

Statistics

5
Total Refusals
4
Unique Violations
7/23/2025
Latest Refusal
9/15/2020
Earliest Refusal

Score Breakdown

Violation Severity
59.1×40%
Refusal Volume
28.8×30%
Recency
76.1×20%
Frequency
10.3×10%
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

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).

32803×

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.

5083×

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.

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
7/23/2025
61LAK40TRAVOPROST (ANTI-COAGULANT)
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)
9/5/2024
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
2/12/2024
86MVNLENS, CONTACT (DISPOSABLE)
508NO 510(K)
Division of Southeast Imports (DSEI)
4/13/2021
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
9/15/2020
65FBJ05WATER, FOR INJECTION, BACTERIOSTATIC, U.S.P. (PHARMACEUTIC AID)
118NOT LISTED
3280FRNMFGREG
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is ALCON MANAGEMENT S.A.'s FDA import refusal history?

ALCON MANAGEMENT S.A. (FEI: 3015911840) has 5 FDA import refusal record(s) in our database, spanning from 9/15/2020 to 7/23/2025.

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. ALCON MANAGEMENT S.A.'s FEI number is 3015911840.

What types of violations has ALCON MANAGEMENT S.A. received?

ALCON MANAGEMENT S.A. 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 ALCON MANAGEMENT S.A. come from?

All FDA import refusal data for ALCON MANAGEMENT S.A. 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.