| Primary Device ID | 00193033442951 |
| NIH Device Record Key | 1be82c01-91b6-46c0-851d-30d5dad428c0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | QUO |
| Version Model Number | 5012796-000.SDM |
| Company DUNS | 062312087 |
| Company Name | FGX INTERNATIONAL INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Phone | +1(401)231-3800 |
| Customerservices@fgxi.com | |
| Phone | +1(401)231-3800 |
| Customerservices@fgxi.com | |
| Phone | +1(401)231-3800 |
| Customerservices@fgxi.com | |
| Phone | +1(401)231-3800 |
| Customerservices@fgxi.com | |
| Phone | +1(401)231-3800 |
| Customerservices@fgxi.com | |
| Phone | +1(401)231-3800 |
| Customerservices@fgxi.com | |
| Phone | +1(401)231-3800 |
| Customerservices@fgxi.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00193033442951 [Primary] |
| HOI | Spectacle, magnifying |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-07-06 |
| Device Publish Date | 2022-06-28 |