| Primary Device ID | 00880304855403 |
| NIH Device Record Key | 676999d2-517d-45ec-abf1-c4d0bae686f2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Distraction Tube - Right |
| Version Model Number | LV01291 |
| Catalog Number | LV01291 |
| Company DUNS | 119260394 |
| Company Name | Highridge Medical, 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 | false |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304855403 [Primary] |
| LXH | Orthopedic manual surgical instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00880304855403]
Moist Heat or Steam Sterilization
[00880304855403]
Moist Heat or Steam Sterilization
[00880304855403]
Moist Heat or Steam Sterilization
[00880304855403]
Moist Heat or Steam Sterilization
[00880304855403]
Moist Heat or Steam Sterilization
[00880304855403]
Moist Heat or Steam Sterilization
[00880304855403]
Moist Heat or Steam Sterilization
[00880304855403]
Moist Heat or Steam Sterilization
[00880304855403]
Moist Heat or Steam Sterilization
[00880304855403]
Moist Heat or Steam Sterilization
[00880304855403]
Moist Heat or Steam Sterilization
[00880304855403]
Moist Heat or Steam Sterilization
[00880304855403]
Moist Heat or Steam Sterilization
[00880304855403]
Moist Heat or Steam Sterilization
[00880304855403]
Moist Heat or Steam Sterilization
[00880304855403]
Moist Heat or Steam Sterilization
[00880304855403]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-05-07 |
| Device Publish Date | 2025-04-29 |
| 03662663082037 - ActivL | 2026-02-11 INF PLATE S1 SZ XL 5DEG SPIKES |
| 03662663082044 - ActivL | 2026-02-11 INF PLATE S1 SIZE XL 5DEG KEEL |
| 03662663082051 - ActivL | 2026-02-11 INF PLATE SIZE XL 0DEG SPIKES |
| 03662663082068 - ActivL | 2026-02-11 SUP PLATE SIZE XL 6DEG SPIKES |
| 03662663082075 - ActivL | 2026-02-11 SUP PLATE SZ XL 11DEG SPIKES |
| 03662663082082 - ActivL | 2026-02-11 INF PLATE SIZE XL 0DEG KEEL |
| 03662663082099 - ActivL | 2026-02-11 SUP PLATE SIZE XL 6DEG KEEL |
| 03662663082105 - ActivL | 2026-02-11 SUP PLATE SIZE XL 11DEG KEEL |