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UltraSound Technologies Ltd.

⚠️ Moderate Risk

FEI: 3003757061 • Caldicot, Gwent • UNITED KINGDOM

FEI

FEI Number

3003757061

📍

Location

Caldicot, Gwent

🇬🇧
🏢

Address

Lodge Way, , Caldicot, Gwent, United Kingdom

Moderate Risk

FDA Import Risk Assessment

28.1
LowModerateHighCritical

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

Statistics

3
Total Refusals
4
Unique Violations
6/18/2010
Latest Refusal
2/20/2002
Earliest Refusal

Score Breakdown

Violation Severity
52.5×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
3.6×10%
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).

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).

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).

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
6/18/2010
85KNGMONITOR, ULTRASONIC, FETAL
118NOT LISTED
341REGISTERED
Southwest Import District Office (SWI-DO)
8/2/2004
85KNGMONITOR, ULTRASONIC, FETAL
508NO 510(K)
Philadelphia District Office (PHI-DO)
2/20/2002
97U09ULTRASOUND PRODUCT FOR NON-MEDICAL USE
476NO REGISTR
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is UltraSound Technologies Ltd.'s FDA import refusal history?

UltraSound Technologies Ltd. (FEI: 3003757061) has 3 FDA import refusal record(s) in our database, spanning from 2/20/2002 to 6/18/2010.

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. UltraSound Technologies Ltd.'s FEI number is 3003757061.

What types of violations has UltraSound Technologies Ltd. received?

UltraSound Technologies Ltd. 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 UltraSound Technologies Ltd. come from?

All FDA import refusal data for UltraSound Technologies 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.