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Lumenis Deutschland Gmbh

⚠️ Moderate Risk

FEI: 3003318392 • Dieburg, Hesse • GERMANY

FEI

FEI Number

3003318392

📍

Location

Dieburg, Hesse

🇩🇪

Country

GERMANY
🏢

Address

Dieselstr. 5b, , Dieburg, Hesse, Germany

Moderate Risk

FDA Import Risk Assessment

26.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
11/7/2002
Latest Refusal
11/7/2002
Earliest Refusal

Score Breakdown

Violation Severity
55.0×40%
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

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).

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
11/7/2002
86LPOGASES USED WITHIN EYE TO PLACE PRESSURE ON DETACHED RETINA
237NO PMA
341REGISTERED
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Lumenis Deutschland Gmbh's FDA import refusal history?

Lumenis Deutschland Gmbh (FEI: 3003318392) has 1 FDA import refusal record(s) in our database, spanning from 11/7/2002 to 11/7/2002.

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. Lumenis Deutschland Gmbh's FEI number is 3003318392.

What types of violations has Lumenis Deutschland Gmbh received?

Lumenis Deutschland Gmbh has been cited for 2 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 Lumenis Deutschland Gmbh come from?

All FDA import refusal data for Lumenis Deutschland Gmbh 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.