ImportRefusal LogoImportRefusal

WUXI XINDI MEDICAL TECHNOLOGY CO., LTD

⚠️ Moderate Risk

FEI: 3030234167 • Wuxi, Jiangsu • CHINA

FEI

FEI Number

3030234167

📍

Location

Wuxi, Jiangsu

🇨🇳

Country

CHINA
🏢

Address

No. 60 Xinfeng Road, Meicun, Town, Xinwu District, Wuxi, Jiangsu, China

Moderate Risk

FDA Import Risk Assessment

44.1
LowModerateHighCritical

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

Statistics

2
Total Refusals
5
Unique Violations
11/6/2025
Latest Refusal
9/23/2025
Earliest Refusal

Score Breakdown

Violation Severity
43.8×40%
Refusal Volume
17.7×30%
Recency
96.5×20%
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).

32802×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

3412×

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).

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

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
11/6/2025
79MDAELASTOMER, SILICONE, FOR SCAR MANAGEMENT
118NOT LISTED
3280FRNMFGREG
333LACKS FIRM
341REGISTERED
Division of West Coast Imports (DWCI)
9/23/2025
79EFQSPONGE, GAUZE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is WUXI XINDI MEDICAL TECHNOLOGY CO., LTD's FDA import refusal history?

WUXI XINDI MEDICAL TECHNOLOGY CO., LTD (FEI: 3030234167) has 2 FDA import refusal record(s) in our database, spanning from 9/23/2025 to 11/6/2025.

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. WUXI XINDI MEDICAL TECHNOLOGY CO., LTD's FEI number is 3030234167.

What types of violations has WUXI XINDI MEDICAL TECHNOLOGY CO., LTD received?

WUXI XINDI MEDICAL TECHNOLOGY CO., LTD has been cited for 5 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 WUXI XINDI MEDICAL TECHNOLOGY CO., LTD come from?

All FDA import refusal data for WUXI XINDI MEDICAL TECHNOLOGY 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.