Essilor Manufacturing
✅ Low Risk
FEI: 1000259259 • Bataan, Central Luzon • PHILIPPINES
FEI Number
1000259259
Location
Bataan, Central Luzon
Country
PHILIPPINESAddress
10 Bepaz, , Bataan, Central Luzon, Philippines
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/28/2005 | 86HQGLENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION) | 341REGISTERED | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Essilor Manufacturing's FDA import refusal history?
Essilor Manufacturing (FEI: 1000259259) has 1 FDA import refusal record(s) in our database, spanning from 2/28/2005 to 2/28/2005.
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. Essilor Manufacturing's FEI number is 1000259259.
What types of violations has Essilor Manufacturing received?
Essilor Manufacturing has been cited for 1 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 Essilor Manufacturing come from?
All FDA import refusal data for Essilor Manufacturing 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.