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Lovehoney-Nice Dream

⚠️ Moderate Risk

FEI: 3012106871 • Shenzhen • CHINA

FEI

FEI Number

3012106871

📍

Location

Shenzhen

🇨🇳

Country

CHINA
🏢

Address

Nice Dream Int Limited No 1, , Shenzhen, , China

Moderate Risk

FDA Import Risk Assessment

39.6
LowModerateHighCritical

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

Statistics

6
Total Refusals
4
Unique Violations
8/2/2016
Latest Refusal
3/24/2016
Earliest Refusal

Score Breakdown

Violation Severity
60.5×40%
Refusal Volume
31.3×30%
Recency
0.0×20%
Frequency
60.0×10%
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

5086×

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.

1185×

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).

165×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

32805×

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.

Refusal History

DateProductViolationsDivision
8/2/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
16DIRECTIONS
508NO 510(K)
Division of Southeast Imports (DSEI)
5/23/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
508NO 510(K)
New Orleans District Office (NOL-DO)
5/9/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
508NO 510(K)
New Orleans District Office (NOL-DO)
4/22/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
New Orleans District Office (NOL-DO)
4/13/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
3/24/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Lovehoney-Nice Dream's FDA import refusal history?

Lovehoney-Nice Dream (FEI: 3012106871) has 6 FDA import refusal record(s) in our database, spanning from 3/24/2016 to 8/2/2016.

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. Lovehoney-Nice Dream's FEI number is 3012106871.

What types of violations has Lovehoney-Nice Dream received?

Lovehoney-Nice Dream 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 Lovehoney-Nice Dream come from?

All FDA import refusal data for Lovehoney-Nice Dream 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.