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HUMANOPTICS HOLDING AG

⚠️ Moderate Risk

FEI: 3010531293 • Sankt Augustin, North Rhine-Westphalia • GERMANY

FEI

FEI Number

3010531293

📍

Location

Sankt Augustin, North Rhine-Westphalia

🇩🇪

Country

GERMANY
🏢

Address

Westerwaldstr. 11-13, , Sankt Augustin, North Rhine-Westphalia, Germany

Moderate Risk

FDA Import Risk Assessment

43.0
LowModerateHighCritical

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

Statistics

2
Total Refusals
4
Unique Violations
3/7/2025
Latest Refusal
6/25/2014
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
17.7×30%
Recency
67.6×20%
Frequency
1.9×10%
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).

23801×

NO PMA/PDP

The article appears to be a class III dev.w/o an approved applic. for premarket approval, and/or a notice of completion of product development protocol filed per section 515(b) or exempt per sect.520(g)(1).

3411×

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).

Refusal History

DateProductViolationsDivision
3/7/2025
86HQLLENS, INTRAOCULAR
237NO PMA
Division of Southeast Imports (DSEI)
6/25/2014
86ODKCORNEAL, REFRACTIVE, IMPLANT
118NOT LISTED
2380NO PMA/PDP
341REGISTERED
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is HUMANOPTICS HOLDING AG's FDA import refusal history?

HUMANOPTICS HOLDING AG (FEI: 3010531293) has 2 FDA import refusal record(s) in our database, spanning from 6/25/2014 to 3/7/2025.

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. HUMANOPTICS HOLDING AG's FEI number is 3010531293.

What types of violations has HUMANOPTICS HOLDING AG received?

HUMANOPTICS HOLDING AG 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 HUMANOPTICS HOLDING AG come from?

All FDA import refusal data for HUMANOPTICS HOLDING AG 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.