LacriPure

GUDID 00853253003195

MENICON AMERICA, INC.

Contact lens wetting solution
Primary Device ID00853253003195
NIH Device Record Key8565699e-235d-49c9-87f2-19e4c8b520ce
Commercial Distribution StatusIn Commercial Distribution
Brand NameLacriPure
Version Model Number98P
Company DUNS034212507
Company NameMENICON AMERICA, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100853253003195 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LPNAccessories, Soft Lens Products

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-01-20
Device Publish Date2016-09-23

On-Brand Devices [LacriPure]

008532530032017P
0085325300319598P

Trademark Results [LacriPure]

Mark Image

Registration | Serial
Company
Trademark
Application Date
LACRIPURE
LACRIPURE
86930894 5172890 Live/Registered
Menicon Co., Ltd.
2016-03-07

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