Primary Device ID | 00850001456128 |
NIH Device Record Key | a640f0cf-4248-4c0d-b03b-0b0ebf3c3bcc |
Commercial Distribution Discontinuation | 2031-07-01 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Juvenis |
Version Model Number | J700B-B |
Company DUNS | 010000704 |
Company Name | Omm Imports Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850001456128 [Primary] |
OHS | Light Based Over The Counter Wrinkle Reduction |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-07-08 |
Device Publish Date | 2022-06-30 |
00850001456128 | Over the counter red/ir device for the treatment of wrinkles. |
00850001456111 | Over the counter red/IR led device for the treatment of wrinkles. |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() JUVENIS 87941129 5741539 Live/Registered |
OMM Imports Inc. 2018-05-30 |
![]() JUVENIS 86145133 not registered Dead/Abandoned |
Juvenis Corporation 2013-12-16 |
![]() JUVENIS 86010816 4558825 Live/Registered |
Erom Inc. 2013-07-15 |