ImportRefusal LogoImportRefusal

Duerr Dental SE

⚠️ Moderate Risk

FEI: 3015509619 • Bietigheim-Bissingen, Baden-Wurttemberg • GERMANY

FEI

FEI Number

3015509619

📍

Location

Bietigheim-Bissingen, Baden-Wurttemberg

🇩🇪

Country

GERMANY
🏢

Address

Hopfigheimer Str. 17, , Bietigheim-Bissingen, Baden-Wurttemberg, Germany

Moderate Risk

FDA Import Risk Assessment

45.6
LowModerateHighCritical

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

Statistics

29
Total Refusals
5
Unique Violations
9/1/2015
Latest Refusal
3/21/2012
Earliest Refusal

Score Breakdown

Violation Severity
51.9×40%
Refusal Volume
54.7×30%
Recency
0.0×20%
Frequency
84.1×10%
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

11828×

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).

34113×

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).

50812×

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.

477×

NON STD

The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.

32805×

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.

Refusal History

DateProductViolationsDivision
9/1/2015
90IZLSYSTEM, X-RAY, MOBILE
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
10/2/2014
76DZPINSTRUMENT, DIAMOND, DENTAL
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Florida District Office (FLA-DO)
10/2/2014
76DZPINSTRUMENT, DIAMOND, DENTAL
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Florida District Office (FLA-DO)
10/2/2014
76DZPINSTRUMENT, DIAMOND, DENTAL
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Florida District Office (FLA-DO)
10/2/2014
76DZPINSTRUMENT, DIAMOND, DENTAL
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Florida District Office (FLA-DO)
9/26/2013
90IZLSYSTEM, X-RAY, MOBILE
118NOT LISTED
Division of Southeast Imports (DSEI)
9/26/2013
90IWNCASSETTE, MEASUREMENT, ARDRAN-CROOKS
118NOT LISTED
Division of Southeast Imports (DSEI)
9/26/2013
90IZLSYSTEM, X-RAY, MOBILE
118NOT LISTED
Division of Southeast Imports (DSEI)
9/26/2013
80MDZCLEANERS, MEDICAL DEVICES
118NOT LISTED
Division of Southeast Imports (DSEI)
9/26/2013
90IWZFILM, RADIOGRAPHIC
118NOT LISTED
Division of Southeast Imports (DSEI)
9/26/2013
90IWNCASSETTE, MEASUREMENT, ARDRAN-CROOKS
118NOT LISTED
Division of Southeast Imports (DSEI)
9/26/2013
90IZLSYSTEM, X-RAY, MOBILE
118NOT LISTED
Division of Southeast Imports (DSEI)
9/26/2013
80MDZCLEANERS, MEDICAL DEVICES
118NOT LISTED
Division of Southeast Imports (DSEI)
9/26/2013
90IWZFILM, RADIOGRAPHIC
118NOT LISTED
Division of Southeast Imports (DSEI)
3/5/2013
90IZLSYSTEM, X-RAY, MOBILE
118NOT LISTED
47NON STD
508NO 510(K)
Florida District Office (FLA-DO)
3/5/2013
90IWZFILM, RADIOGRAPHIC
118NOT LISTED
47NON STD
Florida District Office (FLA-DO)
3/5/2013
90IZLSYSTEM, X-RAY, MOBILE
47NON STD
508NO 510(K)
Florida District Office (FLA-DO)
10/1/2012
90EGYPROCESSOR, RADIOGRAPHIC-FILM, AUTOMATIC, DENTAL
118NOT LISTED
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
10/1/2012
90EGYPROCESSOR, RADIOGRAPHIC-FILM, AUTOMATIC, DENTAL
118NOT LISTED
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
10/1/2012
76DZPINSTRUMENT, DIAMOND, DENTAL
118NOT LISTED
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
7/24/2012
90IWZFILM, RADIOGRAPHIC
118NOT LISTED
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
7/24/2012
90IWZFILM, RADIOGRAPHIC
118NOT LISTED
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
7/24/2012
90IZLSYSTEM, X-RAY, MOBILE
118NOT LISTED
341REGISTERED
47NON STD
508NO 510(K)
Division of Southeast Imports (DSEI)
7/24/2012
90IZLSYSTEM, X-RAY, MOBILE
118NOT LISTED
341REGISTERED
47NON STD
508NO 510(K)
Division of Southeast Imports (DSEI)
7/24/2012
90IZLSYSTEM, X-RAY, MOBILE
118NOT LISTED
341REGISTERED
47NON STD
508NO 510(K)
Division of Southeast Imports (DSEI)
7/24/2012
90IZLSYSTEM, X-RAY, MOBILE
118NOT LISTED
341REGISTERED
47NON STD
508NO 510(K)
Division of Southeast Imports (DSEI)
3/21/2012
90IZLSYSTEM, X-RAY, MOBILE
118NOT LISTED
Division of Southeast Imports (DSEI)
3/21/2012
90IZLSYSTEM, X-RAY, MOBILE
118NOT LISTED
Division of Southeast Imports (DSEI)
3/21/2012
90IZLSYSTEM, X-RAY, MOBILE
118NOT LISTED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Duerr Dental SE's FDA import refusal history?

Duerr Dental SE (FEI: 3015509619) has 29 FDA import refusal record(s) in our database, spanning from 3/21/2012 to 9/1/2015.

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. Duerr Dental SE's FEI number is 3015509619.

What types of violations has Duerr Dental SE received?

Duerr Dental SE has been cited for 5 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 Duerr Dental SE come from?

All FDA import refusal data for Duerr Dental SE 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.