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SHENZHEN S HANDE TECHNOLOGY CO L

⚠️ Moderate Risk

FEI: 3021316147 • Shenzhen • CHINA

FEI

FEI Number

3021316147

📍

Location

Shenzhen

🇨🇳

Country

CHINA
🏢

Address

Bldg 2f, 8 Xinxintian In, Shenzhen, , China

Moderate Risk

FDA Import Risk Assessment

42.6
LowModerateHighCritical

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

Statistics

2
Total Refusals
5
Unique Violations
3/25/2025
Latest Refusal
2/27/2025
Earliest Refusal

Score Breakdown

Violation Severity
54.0×40%
Refusal Volume
17.7×30%
Recency
68.8×20%
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

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).

1261×

FAILS STD

The article appears to be a device which is subject to a performance standard established under Section 514 and does not appear to be in all respects in conformity with such standard.

32801×

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.

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
3/25/2025
79OHTLIGHT BASED OVER-THE-COUNTER HAIR REMOVAL
126FAILS STD
Division of Southeast Imports (DSEI)
2/27/2025
89QPLELECTROMAGNETIC STIMULATOR, PAIN RELIEF
118NOT LISTED
3280FRNMFGREG
333LACKS FIRM
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is SHENZHEN S HANDE TECHNOLOGY CO L's FDA import refusal history?

SHENZHEN S HANDE TECHNOLOGY CO L (FEI: 3021316147) has 2 FDA import refusal record(s) in our database, spanning from 2/27/2025 to 3/25/2025.

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. SHENZHEN S HANDE TECHNOLOGY CO L's FEI number is 3021316147.

What types of violations has SHENZHEN S HANDE TECHNOLOGY CO L received?

SHENZHEN S HANDE TECHNOLOGY CO L 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 SHENZHEN S HANDE TECHNOLOGY CO L come from?

All FDA import refusal data for SHENZHEN S HANDE TECHNOLOGY CO L 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.