ICODI CO., LTD.
⚠️ Moderate Risk
FEI: 3012187418 • Buk-gu, Gwangju Gwangyeogsi • SOUTH KOREA
FEI Number
3012187418
Location
Buk-gu, Gwangju Gwangyeogsi
Country
SOUTH KOREAAddress
2 Cheomdan Venture-ro 60 Beon-Gil, , Buk-gu, Gwangju Gwangyeogsi, South Korea
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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).
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.
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).
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.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/8/2023 | 86LPLLENSES, SOFT CONTACT, DAILY WEAR | Division of Southeast Imports (DSEI) | |
| 2/8/2023 | 86LPLLENSES, SOFT CONTACT, DAILY WEAR | Division of Southeast Imports (DSEI) | |
| 12/16/2022 | 86LPLLENSES, SOFT CONTACT, DAILY WEAR | 2480RXPERSONAL | Division of Southeast Imports (DSEI) |
| 5/23/2019 | 86LPLLENSES, SOFT CONTACT, DAILY WEAR | Division of Southeast Imports (DSEI) | |
| 4/15/2016 | 86MVNLENS, CONTACT (DISPOSABLE) | Seattle District Office (SEA-DO) |
Frequently Asked Questions
What is ICODI CO., LTD.'s FDA import refusal history?
ICODI CO., LTD. (FEI: 3012187418) has 5 FDA import refusal record(s) in our database, spanning from 4/15/2016 to 2/8/2023.
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. ICODI CO., LTD.'s FEI number is 3012187418.
What types of violations has ICODI CO., LTD. received?
ICODI CO., LTD. has been cited for 6 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 ICODI CO., LTD. come from?
All FDA import refusal data for ICODI 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.