FOSTER GRANT 1013131-150.HUD
GUDID 00024021441352
FGX INTERNATIONAL INC.
Prescription spectacles| Primary Device ID | 00024021441352 |
| NIH Device Record Key | dea77487-d748-4158-a155-a7839e452586 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FOSTER GRANT |
| Version Model Number | 1013131-150.HUD |
| Catalog Number | 1013131-150.HUD |
| 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 |
Customer Support Contacts
| 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 | |
| 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 | |
| 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 | |
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00024021441352 [Primary] |
FDA Product Code
| HOI | Spectacle, magnifying |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-09-02 |
| Device Publish Date | 2021-08-25 |
On-Brand Devices [FOSTER GRANT]
Trademark Results [FOSTER GRANT]
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