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MEDIIMPLANTES

⚠️ Moderate Risk

FEI: 3012119325 • Bucaramanga, Santander • COLOMBIA

FEI

FEI Number

3012119325

📍

Location

Bucaramanga, Santander

🇨🇴

Country

COLOMBIA
🏢

Address

Parque Industrial 1 Manzana C Bodega 10, , Bucaramanga, Santander, Colombia

Moderate Risk

FDA Import Risk Assessment

32.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
4/23/2020
Latest Refusal
4/23/2020
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

5081×

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
4/23/2020
87JDNIMPLANT, FIXATION DEVICE, SPINAL
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is MEDIIMPLANTES's FDA import refusal history?

MEDIIMPLANTES (FEI: 3012119325) has 1 FDA import refusal record(s) in our database, spanning from 4/23/2020 to 4/23/2020.

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. MEDIIMPLANTES's FEI number is 3012119325.

What types of violations has MEDIIMPLANTES received?

MEDIIMPLANTES has been cited for 1 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 MEDIIMPLANTES come from?

All FDA import refusal data for MEDIIMPLANTES 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.