| Primary Device ID | 06974308960103 |
| NIH Device Record Key | 65ab1a7d-ffa8-41eb-8f39-de5abb0883e4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Retone |
| Version Model Number | Vigor U 402BT |
| Company DUNS | 544329913 |
| Company Name | Xiamen Retone Hearing Technology Co., Ltd. |
| 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 | false |
| Serial Number | true |
| 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 | 06974308960103 [Primary] |
| QUF | Hearing Aid, Air-Conduction, Over The Counter |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-02-03 |
| Device Publish Date | 2025-01-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() RETONE 97193401 not registered Live/Pending |
Xiamen Retone Hearing Technology Co., Ltd. 2021-12-28 |
![]() RETONE 87103587 5449154 Live/Registered |
RESTORATION DERMACARE LLC 2016-07-14 |