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Karl Storz GMBH & Co KG (KSVEM)

⚠️ Moderate Risk

FEI: 3006453991 • Garching-Hochbruck • GERMANY

FEI

FEI Number

3006453991

📍

Location

Garching-Hochbruck

🇩🇪

Country

GERMANY
🏢

Address

Carl-Von-Linde Str. 15, , Garching-Hochbruck, , Germany

Moderate Risk

FDA Import Risk Assessment

35.9
LowModerateHighCritical

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

Statistics

10
Total Refusals
2
Unique Violations
9/4/2020
Latest Refusal
2/11/2011
Earliest Refusal

Score Breakdown

Violation Severity
58.2×40%
Refusal Volume
38.6×30%
Recency
0.0×20%
Frequency
10.4×10%
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

11810×

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).

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.

Refusal History

DateProductViolationsDivision
9/4/2020
79GCJLAPAROSCOPE, GENERAL & PLASTIC SURGERY
118NOT LISTED
Division of Southeast Imports (DSEI)
1/4/2012
78OCXENDOSCOPIC, IRRIGATION/SUCTION SYSTEM
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
1/4/2012
78FAJCYSTOSCOPE, DIAGNOSTIC
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
1/4/2012
78FETTAPE, TELEVISION & VIDEO, CLOSED-CIRCUIT, USED DURING ENDOSCOPIC PROCEDURE
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
1/4/2012
79GEIDEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
1/4/2012
78FCRLIGHT SOURCE, PHOTOGRAPHIC, FIBEROPTIC
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
1/4/2012
85HIFINSUFFLATOR, LAPAROSCOPIC
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
1/4/2012
74DRCTROCAR
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
1/4/2012
78FCLFORCEPS, BIOPSY, NON-ELECTRIC
118NOT LISTED
New Orleans District Office (NOL-DO)
2/11/2011
79LRWSCISSORS, GENERAL USE, SURGICAL
118NOT LISTED
Detroit District Office (DET-DO)

Frequently Asked Questions

What is Karl Storz GMBH & Co KG (KSVEM)'s FDA import refusal history?

Karl Storz GMBH & Co KG (KSVEM) (FEI: 3006453991) has 10 FDA import refusal record(s) in our database, spanning from 2/11/2011 to 9/4/2020.

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. Karl Storz GMBH & Co KG (KSVEM)'s FEI number is 3006453991.

What types of violations has Karl Storz GMBH & Co KG (KSVEM) received?

Karl Storz GMBH & Co KG (KSVEM) 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 Karl Storz GMBH & Co KG (KSVEM) come from?

All FDA import refusal data for Karl Storz GMBH & Co KG (KSVEM) 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.