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POINTIMPLANT CO., LTD.

⚠️ Moderate Risk

FEI: 3010476612 • Gwangmyeong, Gyeonggi • SOUTH KOREA

FEI

FEI Number

3010476612

📍

Location

Gwangmyeong, Gyeonggi

🇰🇷
🏢

Address

7F, 8F, C dong, 43, Iljik-ro, , Gwangmyeong, Gyeonggi, South Korea

Moderate Risk

FDA Import Risk Assessment

26.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
11/18/2013
Latest Refusal
11/18/2013
Earliest Refusal

Score Breakdown

Violation Severity
55.0×40%
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

1181×

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).

4761×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

Refusal History

DateProductViolationsDivision
11/18/2013
76EHDUNIT, X-RAY, EXTRAORAL WITH TIMER
118NOT LISTED
476NO REGISTR
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is POINTIMPLANT CO., LTD.'s FDA import refusal history?

POINTIMPLANT CO., LTD. (FEI: 3010476612) has 1 FDA import refusal record(s) in our database, spanning from 11/18/2013 to 11/18/2013.

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. POINTIMPLANT CO., LTD.'s FEI number is 3010476612.

What types of violations has POINTIMPLANT CO., LTD. received?

POINTIMPLANT CO., LTD. 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 POINTIMPLANT CO., LTD. come from?

All FDA import refusal data for POINTIMPLANT CO., LTD. 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.