Ann Taylor

GUDID 00730638347221

SUNGLASSES -TYATP912 C01 BLACK 48-21 135C

L'Amy, Incorporated

Tinted non-prescription spectacles
Primary Device ID00730638347221
NIH Device Record Keydd8732c2-45e2-4db7-b513-dbd64f098ff1
Commercial Distribution Discontinuation2027-12-08
Commercial Distribution StatusIn Commercial Distribution
Brand NameAnn Taylor
Version Model NumberTYATP91201
Company DUNS101332278
Company NameL'Amy, Incorporated
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 Perscriptiontrue
OTC Over-The-Countertrue

Customer Support Contacts

Phone2037610611
Emailsupport@lamyamerica.com
Phone2037610611
Emailsupport@lamyamerica.com
Phone2037610611
Emailsupport@lamyamerica.com
Phone2037610611
Emailsupport@lamyamerica.com
Phone2037610611
Emailsupport@lamyamerica.com
Phone2037610611
Emailsupport@lamyamerica.com
Phone2037610611
Emailsupport@lamyamerica.com
Phone2037610611
Emailsupport@lamyamerica.com
Phone2037610611
Emailsupport@lamyamerica.com
Phone2037610611
Emailsupport@lamyamerica.com
Phone2037610611
Emailsupport@lamyamerica.com
Phone2037610611
Emailsupport@lamyamerica.com
Phone2037610611
Emailsupport@lamyamerica.com
Phone2037610611
Emailsupport@lamyamerica.com
Phone2037610611
Emailsupport@lamyamerica.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100730638347221 [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 Date2022-12-12
Device Publish Date2022-12-02