Primary Device ID | 00816063021360 |
NIH Device Record Key | e1c6c682-396b-4944-9447-9ae80cbb678b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ClinCheck |
Version Model Number | SW-0000159 |
Company DUNS | 013831768 |
Company Name | ALIGN TECHNOLOGY, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816063021360 [Primary] |
NXC | Aligner, Sequential |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-02-25 |
Device Publish Date | 2022-02-17 |
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Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CLINCHECK 88016081 not registered Live/Pending |
Align Technology, Inc. 2018-06-26 |
CLINCHECK 78576566 3366656 Live/Registered |
Align Technology, Inc. 2005-02-28 |
CLINCHECK 75695982 2392324 Live/Registered |
Align Technology, Inc. 1999-05-03 |
CLINCHECK 75268222 2202588 Dead/Cancelled |
CROSS COUNTRY HEALTHCARE, INC. 1997-04-02 |