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Kulzer Gmbh

⚠️ Moderate Risk

FEI: 3002807166 • Wehrheim, Hassia • GERMANY

FEI

FEI Number

3002807166

📍

Location

Wehrheim, Hassia

🇩🇪

Country

GERMANY
🏢

Address

Philipp-Reis-Str. 8/13, , Wehrheim, Hassia, Germany

Moderate Risk

FDA Import Risk Assessment

46.3
LowModerateHighCritical

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

Statistics

9
Total Refusals
4
Unique Violations
4/18/2025
Latest Refusal
5/28/2015
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
37.0×30%
Recency
71.1×20%
Frequency
9.1×10%
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

1188×

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).

32807×

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.

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).

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
4/18/2025
76LFESOLUTION, COLD STERILIZING
118NOT LISTED
3280FRNMFGREG
Division of West Coast Imports (DWCI)
8/19/2024
76KLEAGENT, TOOTH BONDING, RESIN
118NOT LISTED
Division of Northeast Imports (DNEI)
10/18/2023
76KLEAGENT, TOOTH BONDING, RESIN
118NOT LISTED
3280FRNMFGREG
Division of Northeast Imports (DNEI)
10/18/2023
76KLEAGENT, TOOTH BONDING, RESIN
118NOT LISTED
3280FRNMFGREG
Division of Northeast Imports (DNEI)
10/18/2023
76EBFMATERIAL, TOOTH SHADE, RESIN
118NOT LISTED
3280FRNMFGREG
Division of Northeast Imports (DNEI)
10/18/2023
76KLEAGENT, TOOTH BONDING, RESIN
118NOT LISTED
3280FRNMFGREG
Division of Northeast Imports (DNEI)
2/12/2019
76EBFMATERIAL, TOOTH SHADE, RESIN
3280FRNMFGREG
341REGISTERED
Division of Northeast Imports (DNEI)
1/29/2018
76EBFMATERIAL, TOOTH SHADE, RESIN
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
5/28/2015
76EMACEMENT, DENTAL
118NOT LISTED
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Kulzer Gmbh's FDA import refusal history?

Kulzer Gmbh (FEI: 3002807166) has 9 FDA import refusal record(s) in our database, spanning from 5/28/2015 to 4/18/2025.

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. Kulzer Gmbh's FEI number is 3002807166.

What types of violations has Kulzer Gmbh received?

Kulzer Gmbh 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 Kulzer Gmbh come from?

All FDA import refusal data for Kulzer 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.