FOSTER GRANT

GUDID 00031568629952

FGX INTERNATIONAL INC.

Prescription spectacles

• Primary Device ID: 00031568629952
• NIH Device Record Key: ce06c60a-b809-4962-b698-9515b057172b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FOSTER GRANT
• Version Model Number: 5014175-150.CGU
• 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
• Email: Customerservices@fgxi.com
• Phone: +1(401)231-3800
• Email: Customerservices@fgxi.com
• Phone: +1(401)231-3800
• Email: Customerservices@fgxi.com
• Phone: +1(401)231-3800
• Email: Customerservices@fgxi.com
• Phone: +1(401)231-3800
• Email: Customerservices@fgxi.com
• Phone: +1(401)231-3800
• Email: Customerservices@fgxi.com
• Phone: +1(401)231-3800
• Email: Customerservices@fgxi.com
• Phone: +1(401)231-3800
• Email: Customerservices@fgxi.com
• Phone: +1(401)231-3800
• Email: Customerservices@fgxi.com
• Phone: +1(401)231-3800
• Email: Customerservices@fgxi.com
• Phone: +1(401)231-3800
• Email: Customerservices@fgxi.com
• Phone: +1(401)231-3800
• Email: Customerservices@fgxi.com
• Phone: +1(401)231-3800
• Email: Customerservices@fgxi.com
• Phone: +1(401)231-3800
• Email: Customerservices@fgxi.com
• Phone: +1(401)231-3800
• Email: Customerservices@fgxi.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00031568629952 [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: 2022-10-19
• Device Publish Date: 2022-10-11

On-Brand Devices [FOSTER GRANT]

• 00031568411670: 10206135.MCV
• 00031568410741: 10206138.MCV
• 00031568405549: 10206123.MCV
• 00024021441376: 1013131-200.HUD
• 00024021441352: 1013131-150.HUD
• 00024021441345: 1013131-125.HUD
• 00193033024157: 10244921.FGX
• 00193033023549: 10244915.FGX
• 00193033021439: 10245691.CGR
• 00193033021415: 10245620.CGR
• 00193033021378: 10245616.CGR
• 00193033021361: 10245615.CGR
• 00193033019368: 10245030.MCV
• 00193033019351: 10245029.MCV
• 00193033019276: 10245021.MCV
• 00193033019269: 10245020.MCV
• 00193033019221: 10245016.MCV
• 00193033019214: 10245015.MCV
• 00193033018910: 1019270-300.COM
• 00193033018903: 1019270-250.COM
• 00193033018897: 1019270-200.COM
• 00193033018880: 1019270-150.COM
• 00193033018217: 1019559-275.FDG
• 00193033018200: 1019559-250.FDG
• 00193033018187: 1019559-200.FDG
• 00193033018170: 1019559-175.FDG
• 00193033018156: 1019559-150.FDG
• 00193033018132: 1019559-125.FDG
• 00193033014769: 1019602-325.ARM
• 00193033014752: 1019602-275.ARM
• 00193033014745: 1019602-250.ARM
• 00193033014738: 1019602-200.ARM
• 00193033014721: 1019602-150.ARM
• 00193033014714: 1019602-125.ARM
• 00193033014707: 1019603-325.ARM
• 00193033014691: 1019603-275.ARM
• 00193033014684: 1019603-250.ARM
• 00193033014677: 1019603-200.ARM
• 00193033014660: 1019603-150.ARM
• 00193033014653: 1019603-125.ARM
• 00193033002261: 1019442-325.ARM
• 00193033002254: 1019442-275.ARM
• 00193033002247: 1019442-250.ARM
• 00193033002230: 1019442-200.ARM
• 00193033002223: 1019442-150.ARM
• 00193033002216: 1019442-125.ARM
• 00031568873898: 10400666.FDG
• 00031568873171: 10400670.FDG
• 00031568873089: 10400671.FDG
• 00031568873041: 10400668.FDG