QUO

GUDID 00057800255505

FGX INTERNATIONAL INC.

Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles Tinted non-prescription spectacles
Primary Device ID00057800255505
NIH Device Record Keyb7a827ae-982a-4c9b-85e5-42fbb9edb990
Commercial Distribution StatusIn Commercial Distribution
Brand NameQUO
Version Model Number10265182.SDM
Company DUNS062312087
Company NameFGX INTERNATIONAL INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100057800255505 [Primary]

FDA Product Code

HQYSunglasses (non-prescription including photosensitive)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-10-19
Device Publish Date2022-10-11

On-Brand Devices [QUO]

0019303320799410252522.SDM
0019303320720810251063.SDM
001930335808825014361-000.SDM
001930335808755014358-000.SDM
001930335808685014360-000.SDM
001930335808515014357-000.SDM
001930335808445014359-000.SDM
0019303350802210262843.SDM
0019303350801510262849.SDM
0019303350800810262848.SDM
0019303350799510262847.SDM
0019303350798810262856.SDM
0019303350797110262855.SDM
0019303350796410262865.SDM
0019303350795710262852.SDM
0019303350794010262854.SDM
0019303350793310262857.SDM
0019303350792610262846.SDM
0019303350791910262844.SDM
0019303350790210262850.SDM
0019303350789610262845.SDM
0019303350787210262851.SDM
0019303350786510262853.SDM
0019303346448910260314.SDM
0019303346447210260313.SDM
0019303346446510260254.SDM
0019303346445810260252.SDM
0019303346444110260263.SDM
0019303346443410260270.SDM
0019303346442710260269.SDM
0019303346441010260268.SDM
0019303346440310260267.SDM
0019303346439710260265.SDM
0019303346438010260264.SDM
0019303346437310260261.SDM
0019303346436610260260.SDM
0019303346435910260259.SDM
0019303346434210260258.SDM
0019303346433510260257.SDM
0019303346432810260256.SDM
0019303346431110260255.SDM
0019303346430410260253.SDM
0019303346429810260251.SDM
001930334430025012792-000.SDM
001930334429995012798-000.SDM
001930334429825012800-000.SDM
001930334429755012794-000.SDM
001930334429685012799-000.SDM
001930334429515012796-000.SDM
001930334429445012797-000.SDM

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