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ORANTECH INC

⚠️ High Risk

FEI: 3013783488 • Shenzhen, Guangdon • CHINA

FEI

FEI Number

3013783488

📍

Location

Shenzhen, Guangdon

🇨🇳

Country

CHINA
🏢

Address

Zone#A,4f,1st Bld,7th Industrial Zone,Yulv Community, Gongming, Guangming New District, , Shenzhen, Guangdon, China

High Risk

FDA Import Risk Assessment

56.3
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

12
Total Refusals
5
Unique Violations
12/9/2025
Latest Refusal
4/12/2019
Earliest Refusal

Score Breakdown

Violation Severity
56.2×40%
Refusal Volume
41.3×30%
Recency
98.3×20%
Frequency
18.0×10%
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

5089×

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).

32803×

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.

2371×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

Refusal History

DateProductViolationsDivision
12/9/2025
73DQAOXIMETER
508NO 510(K)
Division of Southeast Imports (DSEI)
9/30/2025
73DQAOXIMETER
508NO 510(K)
Division of Southeast Imports (DSEI)
12/22/2023
73DQAOXIMETER
237NO PMA
Division of West Coast Imports (DWCI)
5/2/2022
85HGMSYSTEM, MONITORING, PERINATAL
118NOT LISTED
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
1/7/2022
73DQAOXIMETER
508NO 510(K)
Division of Southwest Imports (DSWI)
12/22/2021
73DQAOXIMETER
508NO 510(K)
Division of Southeast Imports (DSEI)
12/22/2021
73DQAOXIMETER
508NO 510(K)
Division of Southeast Imports (DSEI)
12/21/2021
73DQAOXIMETER
508NO 510(K)
Division of Southeast Imports (DSEI)
12/16/2021
73DQAOXIMETER
508NO 510(K)
Division of Southeast Imports (DSEI)
4/12/2019
80FRNPUMP, INFUSION
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Northern Border Imports (DNBI)
4/12/2019
80FRNPUMP, INFUSION
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Division of Northern Border Imports (DNBI)
4/12/2019
80FOXSTAND, INFUSION
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is ORANTECH INC's FDA import refusal history?

ORANTECH INC (FEI: 3013783488) has 12 FDA import refusal record(s) in our database, spanning from 4/12/2019 to 12/9/2025.

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. ORANTECH INC's FEI number is 3013783488.

What types of violations has ORANTECH INC received?

ORANTECH INC 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 ORANTECH INC come from?

All FDA import refusal data for ORANTECH INC 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.