ImportRefusal LogoImportRefusal

Martin Medizin-Technik

⚠️ Moderate Risk

FEI: 2862 • Tuttlingen, Baden-Wurttemberg • GERMANY

FEI

FEI Number

2862

📍

Location

Tuttlingen, Baden-Wurttemberg

🇩🇪

Country

GERMANY
🏢

Address

Ludwigstaler Str. 132, , Tuttlingen, Baden-Wurttemberg, 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

13
Total Refusals
3
Unique Violations
12/20/2005
Latest Refusal
11/15/2001
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
42.5×30%
Recency
0.0×20%
Frequency
31.7×10%
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

34112×

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.

1182×

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).

Refusal History

DateProductViolationsDivision
12/20/2005
79FTNKIT, PLASTIC SURGERY AND ACCESSORIES
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
12/20/2005
79GDGHOOK, SURGICAL, GENERAL & PLASTIC SURGERY
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
12/20/2005
79FZYHAMMER, SURGICAL
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
12/20/2005
79GENFORCEPS, GENERAL & PLASTIC SURGERY
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
12/20/2005
79GDFGUIDE, NEEDLE, SURGICAL
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
12/20/2005
79GDJCLAMP, SURGICAL, GENERAL & PLASTIC SURGERY
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
12/20/2005
79GENFORCEPS, GENERAL & PLASTIC SURGERY
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
12/20/2005
79GEGELEVATOR, SURGICAL, GENERAL & PLASTIC SURGERY
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
12/20/2005
79LRWSCISSORS, GENERAL USE, SURGICAL
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
12/20/2005
79EMFKNIFE, SURGICAL
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
12/20/2005
74DPSELECTROCARDIOGRAPH
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
4/8/2002
79MDWINSTRUMENT, MANUAL, SURGICAL, GENERAL USE
118NOT LISTED
Florida District Office (FLA-DO)
11/15/2001
79MDWINSTRUMENT, MANUAL, SURGICAL, GENERAL USE
118NOT LISTED
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Martin Medizin-Technik's FDA import refusal history?

Martin Medizin-Technik (FEI: 2862) has 13 FDA import refusal record(s) in our database, spanning from 11/15/2001 to 12/20/2005.

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. Martin Medizin-Technik's FEI number is 2862.

What types of violations has Martin Medizin-Technik received?

Martin Medizin-Technik has been cited for 3 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 Martin Medizin-Technik come from?

All FDA import refusal data for Martin Medizin-Technik 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.