Primary Device ID | 00852673007080 |
NIH Device Record Key | 0958cc5d-9af9-44fc-bb5d-10a108676728 |
Commercial Distribution Discontinuation | 2019-11-15 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Propel |
Version Model Number | ASM-20018-04 |
Catalog Number | ASM-20018-04 |
Company DUNS | 117334253 |
Company Name | PROPEL ORTHODONTICS LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
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 |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00852673007080 [Primary] |
ECR | Setter, Band, Orthodontic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-01-23 |
Device Publish Date | 2018-03-09 |
00852673007097 | VPro+ |
00852673007080 | C-Shaped Vibration Device, Brazil |
00852673007073 | Packaged C-Shaped Mouthpiece, Tapered, Assy |
00852673007066 | Packaged Mouthpiece, Single, Assy |
00852673007059 | Assy. Packaged Disposable Drill Tip-Open |
00852673007042 | Propel, Reusable Handle |
00852673007035 | Assy. Packaged Disposable Drill Tip, Closed |
00852673007028 | Assy. Packaged Perforation Device, Contra-Angle |
00852673007011 | C-Shaped Vibration Device |
00852673007004 | Perforation Device, Propel XL |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PROPEL 98794068 not registered Live/Pending |
Propel, Inc. 2024-10-10 |
PROPEL 98745882 not registered Live/Pending |
CUETEC CO., LIMITED 2024-09-11 |
PROPEL 98625025 not registered Live/Pending |
HCPro LLC 2024-06-28 |
PROPEL 98385072 not registered Live/Pending |
Les Composites Motion Inc. 2024-01-31 |
PROPEL 98384146 not registered Live/Pending |
Lydonia Technologies, LLC 2024-01-31 |
PROPEL 98102956 not registered Live/Pending |
The Visibility Company 2023-07-26 |
PROPEL 97917479 not registered Live/Pending |
Seachem Laboratories, Inc. 2023-05-02 |
PROPEL 97804321 not registered Live/Pending |
Propel Holdings, LLC 2023-02-21 |
PROPEL 97766658 not registered Live/Pending |
ENGS Commercial Finance Co 2023-01-24 |
PROPEL 97662890 not registered Live/Pending |
Vita-Mix Management Corporation 2022-11-07 |
PROPEL 97657300 not registered Live/Pending |
Saietta Group PLC 2022-11-01 |
PROPEL 97636421 not registered Live/Pending |
Stokely-Van Camp, Inc. 2022-10-18 |