Primary Device ID | H6683524870 |
NIH Device Record Key | 9fd2431d-f1a1-4f53-8542-a63b3add13c5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Omni |
Version Model Number | 24-42947 |
Catalog Number | 24-42947 |
Company DUNS | 073503117 |
Company Name | Keystone Industries |
Device Count | 200 |
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 | true |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)333-3131 |
tschwear@keystoneind.com | |
Phone | +1(800)333-3131 |
tschwear@keystoneind.com | |
Phone | +1(800)333-3131 |
tschwear@keystoneind.com | |
Phone | +1(800)333-3131 |
tschwear@keystoneind.com | |
Phone | +1(800)333-3131 |
tschwear@keystoneind.com | |
Phone | +1(800)333-3131 |
tschwear@keystoneind.com | |
Phone | +1(800)333-3131 |
tschwear@keystoneind.com | |
Phone | +1(800)333-3131 |
tschwear@keystoneind.com | |
Phone | +1(800)333-3131 |
tschwear@keystoneind.com | |
Phone | +1(800)333-3131 |
tschwear@keystoneind.com | |
Phone | +1(800)333-3131 |
tschwear@keystoneind.com | |
Phone | +1(800)333-3131 |
tschwear@keystoneind.com | |
Phone | +1(800)333-3131 |
tschwear@keystoneind.com | |
Phone | +1(800)333-3131 |
tschwear@keystoneind.com | |
Phone | +1(800)333-3131 |
tschwear@keystoneind.com | |
Phone | +1(800)333-3131 |
tschwear@keystoneind.com | |
Phone | +1(800)333-3131 |
tschwear@keystoneind.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | H6683524870 [Unit of Use] |
HIBCC | H6683524871 [Primary] |
EJR | AGENT, POLISHING, ABRASIVE, ORAL CAVITY |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-07-01 |
Device Publish Date | 2024-06-21 |
H6683524840 | Prophy Paste Bubble Gum Fine Box/200 |
H6683524830 | Prophy Paste Cherry Coarse Box/200 |
H6683524820 | Prophy Paste Cherry Medium Box/200 |
H6683524810 | Prophy Paste Mint Coarse Box/200 |
H6683524800 | Prophy Paste Mint Medium Box/200 |
H6683524880 | Prophy Paste Assorted Coarse Box/200 |
H6683524870 | Prophy Paste Assorted Medium Box/200 |
H6683524860 | Prophy Paste Bubble Gum Coarse Box/200 |
H6683524850 | Prophy Paste Bubble Gum Medium Box/200 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
OMNI 98768534 not registered Live/Pending |
OmniMetrix, LLC 2024-09-25 |
OMNI 98611364 not registered Live/Pending |
Gravity Brands Limited 2024-06-20 |
OMNI 98504606 not registered Live/Pending |
OmniOrder 2024-04-17 |
OMNI 98408810 not registered Live/Pending |
Canby Telephone Association 2024-02-16 |
OMNI 98408809 not registered Live/Pending |
Canby Telephone Association 2024-02-16 |
OMNI 98382458 not registered Live/Pending |
Universal Instruments Corporation 2024-01-30 |
OMNI 98374513 not registered Live/Pending |
Tractian LLC 2024-01-24 |
OMNI 98323987 not registered Live/Pending |
IVISION TECH INC. 2023-12-20 |
OMNI 98294861 not registered Live/Pending |
IVISION TECH, Inc. 2023-12-01 |
OMNI 98292411 not registered Live/Pending |
ChargePoint, Inc. 2023-11-30 |
OMNI 98291159 not registered Live/Pending |
Remarc Vending, LLC 2023-11-29 |
OMNI 98275945 not registered Live/Pending |
IVISION TECH, Inc. 2023-11-17 |