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Arthrex Latin America

⚠️ Moderate Risk

FEI: 3005176907 • Col. Florida, Hidalgo • MEXICO

FEI

FEI Number

3005176907

📍

Location

Col. Florida, Hidalgo

🇲🇽

Country

MEXICO
🏢

Address

Calle Insurgentes Sur 600, Huejutla De Reyes, Col. Florida, Hidalgo, Mexico

Moderate Risk

FDA Import Risk Assessment

31.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
7/25/2005
Latest Refusal
7/25/2005
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

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).

5082×

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
7/25/2005
84HBDHANDPIECE (BRACE), DRILL
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
7/25/2005
87HRXARTHROSCOPE AND ACCESSORIES
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Arthrex Latin America's FDA import refusal history?

Arthrex Latin America (FEI: 3005176907) has 2 FDA import refusal record(s) in our database, spanning from 7/25/2005 to 7/25/2005.

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. Arthrex Latin America's FEI number is 3005176907.

What types of violations has Arthrex Latin America received?

Arthrex Latin America 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 Arthrex Latin America come from?

All FDA import refusal data for Arthrex Latin America 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.