| Primary Device ID | 00860012465033 |
| NIH Device Record Key | 91738405-9dd0-4e9a-a746-57b21facbae5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RedRevive |
| Version Model Number | TFX LT1000N |
| Company DUNS | 202099070 |
| Company Name | ToeFX Inc |
| 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 | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860012465033 [Primary] |
| ILY | Lamp, Infrared, Therapeutic Heating |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-12-11 |
| Device Publish Date | 2025-12-03 |
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| 00860012465033 - RedRevive | 2025-12-11 |
| 00860012465033 - RedRevive | 2025-12-11 |
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