US IOL, Inc
FDA Regulatory Profile
US IOL, Inc has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Jun 5, 2025 · NAI
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Summary
Record counts and when each FDA source was last refreshed
| Records | Count | Last refreshed | Source as of | Status |
|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
|---|
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
|---|
| Inspections | 5 | Nov 11, 2026 | Newest record Nov 5, 2026 | Current |
|---|
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
|---|
Related names
| Name | Recalls | 510(k) | Inspections | Compliance | Most recent recall |
|---|
U.S. Iol
Same company group | 0 | 4 | 0 | 0 | — |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|
| Jun 5, 2025 | Lexington, KY | Devices | No Action Indicated (NAI) | 1037089 |
| Aug 28, 2019 | Lexington, KY | Devices | No Action Indicated (NAI) | 1037089 |
| Jun 8, 2016 | Lexington, KY | Devices | No Action Indicated (NAI) | 1037089 |
| Oct 9, 2012 | Lexington, KY | Devices | No Action Indicated (NAI) | 1037089 |
| Dec 16, 2009 | Lexington, KY | Devices | Voluntary Action Indicated (VAI) | 1037089 |
NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|
| FEI 1037089 | Lexington, KY | 5 | Jun 5, 2025 |