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Bioland Technology Ltd.

⚠️ Moderate Risk

FEI: 3004101980 • Shenzhen, Guangdong • CHINA

FEI

FEI Number

3004101980

📍

Location

Shenzhen, Guangdong

🇨🇳

Country

CHINA
🏢

Address

No. A6B7(Block G) ShangRong Industrial Zone No.5 Baolong Road, Baolong Community Longgang District, Shenzhen, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

46.6
LowModerateHighCritical

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

Statistics

5
Total Refusals
4
Unique Violations
7/21/2025
Latest Refusal
4/19/2023
Earliest Refusal

Score Breakdown

Violation Severity
51.3×40%
Refusal Volume
28.8×30%
Recency
76.0×20%
Frequency
22.1×10%
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

5085×

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.

1184×

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).

3414×

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).

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.

Refusal History

DateProductViolationsDivision
7/21/2025
75NBWSYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER
118NOT LISTED
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
7/21/2025
75NBWSYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER
118NOT LISTED
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
5/30/2025
75NBWSYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER
508NO 510(K)
Division of Southeast Imports (DSEI)
5/22/2024
78NTZSTRIP, DIALYSATE, PH, BICARBONATE, GLUCOSE, ACID, INDICATOR
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
4/19/2023
75NBWSYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Bioland Technology Ltd.'s FDA import refusal history?

Bioland Technology Ltd. (FEI: 3004101980) has 5 FDA import refusal record(s) in our database, spanning from 4/19/2023 to 7/21/2025.

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. Bioland Technology Ltd.'s FEI number is 3004101980.

What types of violations has Bioland Technology Ltd. received?

Bioland Technology 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 Bioland Technology Ltd. come from?

All FDA import refusal data for Bioland Technology 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.