Clarity™ Aligners 358-452

GUDID 00652221236500

3M™ Retainer - Single Arch

3M UNITEK CORPORATION

Orthodontic appliance system, progressive
Primary Device ID00652221236500
NIH Device Record Key814142b6-d46d-4210-8dd4-cf60c836a2a5
Commercial Distribution StatusIn Commercial Distribution
Brand NameClarity™ Aligners
Version Model Number358-452
Catalog Number358-452
Company DUNS008256356
Company Name3M UNITEK CORPORATION
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)423-4588
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)423-4588
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)423-4588
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)423-4588
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)423-4588
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)423-4588
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)423-4588
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)423-4588
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)423-4588
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)423-4588
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)423-4588
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)423-4588
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)423-4588
Email3Mhealthcarecompliance@mmm.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100652221236500 [Primary]

FDA Product Code

NXCAligner, sequential

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-12-20

On-Brand Devices [Clarity™ Aligners]

006522212366093M™ Clarity™ Aligner Systems
006522212365933M™ Clarity™ Retainers
006522212365863M™ Clarity™ Aligner Attachment Templates
006522212365793M™ Clarity™ Aligners
006522212365003M™ Retainer - Single Arch
006522212364943M™ Retainer - Dual Arch
006522212364873M™ Clarity™ Aligner Replacement
006522212364703M™ Clarity™ Aligner - Single Arch
006522212364633M™ Clarity™ Aligner - Dual Arch
006522212364563M™ Clarity™ Aligner Attachment Template - Single Arch
006522212364493M™ Clarity™ Aligner Attachment Template - Dual Arch
006522212364323M™ Clarity™ Aligner Replacement - Lost/Damaged
006522212364253M™ Clarity™ Aligner Refinement - Single Arch
006522212364183M™ Clarity™ Aligner Refinement - Dual Arch

Trademark Results [Clarity]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CLARITY
CLARITY
98794066 not registered Live/Pending
Solventum Intellectual Properties Company
2024-10-10
CLARITY
CLARITY
98718262 not registered Live/Pending
Groben, Mason C.
2024-08-26
CLARITY
CLARITY
98647012 not registered Live/Pending
Clarity Movement Co.
2024-07-13
CLARITY
CLARITY
98641763 not registered Live/Pending
Clarity Pharmaceuticals Ltd
2024-07-10
CLARITY
CLARITY
98519512 not registered Live/Pending
Solventum Intellectual Properties Company
2024-04-25
CLARITY
CLARITY
98449573 not registered Live/Pending
A & A Drug Co.
2024-03-14
CLARITY
CLARITY
98405327 not registered Live/Pending
Pitney Bowes Inc.
2024-02-14
CLARITY
CLARITY
98352796 not registered Live/Pending
Precision Planting LLC
2024-01-11
CLARITY
CLARITY
98260471 not registered Live/Pending
Quorum Cyber Security Limited
2023-11-08
CLARITY
CLARITY
98260047 not registered Live/Pending
Fuelling, Adam D
2023-11-08
CLARITY
CLARITY
98258687 not registered Live/Pending
Magi, Inc.
2023-11-07
CLARITY
CLARITY
98258327 not registered Live/Pending
Ceribell, Inc.
2023-11-07

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.