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DIVES MED GMBH SCHONHAUSER

⚠️ High Risk

FEI: 3030400697 • Berlin, Berlin • GERMANY

FEI

FEI Number

3030400697

📍

Location

Berlin, Berlin

🇩🇪

Country

GERMANY
🏢

Address

Allerstr. 10-11, , Berlin, Berlin, Germany

High Risk

FDA Import Risk Assessment

58.1
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

9
Total Refusals
5
Unique Violations
2/20/2025
Latest Refusal
8/7/2024
Earliest Refusal

Score Breakdown

Violation Severity
61.1×40%
Refusal Volume
37.0×30%
Recency
68.0×20%
Frequency
90.0×10%
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

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).

32808×

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.

5087×

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.

2373×

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).

752×

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
2/20/2025
53LY06MOISTURIZING (SKIN CARE PREPARATIONS)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
2/20/2025
53LY06MOISTURIZING (SKIN CARE PREPARATIONS)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
2/20/2025
53LY06MOISTURIZING (SKIN CARE PREPARATIONS)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
2/20/2025
53LY06MOISTURIZING (SKIN CARE PREPARATIONS)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
2/20/2025
53LY06MOISTURIZING (SKIN CARE PREPARATIONS)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
9/27/2024
53YY99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C.
118NOT LISTED
237NO PMA
3280FRNMFGREG
75UNAPPROVED
Division of Southeast Imports (DSEI)
9/18/2024
66VIY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/7/2024
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
118NOT LISTED
237NO PMA
3280FRNMFGREG
508NO 510(K)
Division of Northeast Imports (DNEI)
8/7/2024
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
118NOT LISTED
237NO PMA
3280FRNMFGREG
508NO 510(K)
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is DIVES MED GMBH SCHONHAUSER's FDA import refusal history?

DIVES MED GMBH SCHONHAUSER (FEI: 3030400697) has 9 FDA import refusal record(s) in our database, spanning from 8/7/2024 to 2/20/2025.

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. DIVES MED GMBH SCHONHAUSER's FEI number is 3030400697.

What types of violations has DIVES MED GMBH SCHONHAUSER received?

DIVES MED GMBH SCHONHAUSER 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 DIVES MED GMBH SCHONHAUSER come from?

All FDA import refusal data for DIVES MED GMBH SCHONHAUSER 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.