ImportRefusal LogoImportRefusal

Tecnodisco Sa

⚠️ Moderate Risk

FEI: 3008892760 • Madrid, Madrid • SPAIN

FEI

FEI Number

3008892760

📍

Location

Madrid, Madrid

🇪🇸

Country

SPAIN
🏢

Address

Calle Las Americas 2 Bis, , Madrid, Madrid, Spain

Moderate Risk

FDA Import Risk Assessment

44.2
LowModerateHighCritical

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

Statistics

18
Total Refusals
4
Unique Violations
9/13/2013
Latest Refusal
8/15/2013
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
47.4×30%
Recency
0.0×20%
Frequency
100.0×10%
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

11818×

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).

328018×

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.

34118×

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).

50818×

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
9/13/2013
85HISCONDOM
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
9/13/2013
85NUCLUBRICANT, PATIENT, VAGINAL, LATEX COMPATIBLE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
9/13/2013
85HISCONDOM
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
9/13/2013
80LLIBED, THERAPEUTIC, AC-POWERED, ADJUSTABLE HOME-USE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
9/13/2013
80LLIBED, THERAPEUTIC, AC-POWERED, ADJUSTABLE HOME-USE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
9/13/2013
80LLIBED, THERAPEUTIC, AC-POWERED, ADJUSTABLE HOME-USE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
9/13/2013
80LLIBED, THERAPEUTIC, AC-POWERED, ADJUSTABLE HOME-USE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
9/13/2013
80LLIBED, THERAPEUTIC, AC-POWERED, ADJUSTABLE HOME-USE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
9/13/2013
80FNGLIFT, PATIENT, AC-POWERED
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
8/15/2013
85HISCONDOM
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
8/15/2013
85NUCLUBRICANT, PATIENT, VAGINAL, LATEX COMPATIBLE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
8/15/2013
85HISCONDOM
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
8/15/2013
80LLIBED, THERAPEUTIC, AC-POWERED, ADJUSTABLE HOME-USE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
8/15/2013
80LLIBED, THERAPEUTIC, AC-POWERED, ADJUSTABLE HOME-USE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
8/15/2013
80LLIBED, THERAPEUTIC, AC-POWERED, ADJUSTABLE HOME-USE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
8/15/2013
80LLIBED, THERAPEUTIC, AC-POWERED, ADJUSTABLE HOME-USE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
8/15/2013
80LLIBED, THERAPEUTIC, AC-POWERED, ADJUSTABLE HOME-USE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
8/15/2013
80FNGLIFT, PATIENT, AC-POWERED
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Tecnodisco Sa's FDA import refusal history?

Tecnodisco Sa (FEI: 3008892760) has 18 FDA import refusal record(s) in our database, spanning from 8/15/2013 to 9/13/2013.

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. Tecnodisco Sa's FEI number is 3008892760.

What types of violations has Tecnodisco Sa received?

Tecnodisco Sa 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 Tecnodisco Sa come from?

All FDA import refusal data for Tecnodisco Sa 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.