ImportRefusal LogoImportRefusal

Medica Tcpc

⚠️ Moderate Risk

FEI: 3004020084 • Dubai • UNITED ARAB EMIRATES

FEI

FEI Number

3004020084

📍

Location

Dubai

🇦🇪
🏢

Address

Dubai Airport, , Dubai, , United Arab Emirates

Moderate Risk

FDA Import Risk Assessment

33.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
4
Unique Violations
5/24/2004
Latest Refusal
6/5/2003
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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).

2372×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

3411×

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).

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
5/24/2004
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
118NOT LISTED
341REGISTERED
508NO 510(K)
Cincinnati District Office (CIN-DO)
1/20/2004
89LZXACID, SODIUM HYALURONIC, INTRA-ARTICULAR
237NO PMA
New York District Office (NYK-DO)
6/5/2003
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
118NOT LISTED
237NO PMA
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is Medica Tcpc's FDA import refusal history?

Medica Tcpc (FEI: 3004020084) has 3 FDA import refusal record(s) in our database, spanning from 6/5/2003 to 5/24/2004.

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. Medica Tcpc's FEI number is 3004020084.

What types of violations has Medica Tcpc received?

Medica Tcpc 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 Medica Tcpc come from?

All FDA import refusal data for Medica Tcpc 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.