| Primary Device ID | 00840277405630 |
| NIH Device Record Key | c1f49ce5-d8de-48a8-b75b-21573812699a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Strut Suture |
| Version Model Number | 103.000 |
| Company DUNS | 964053560 |
| Company Name | RIVERPOINT MEDICAL, LLC |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| 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 | 00840277405630 [Primary] |
| MBI | Fastener, Fixation, Nondegradable, Soft Tissue |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-03-27 |
| Device Publish Date | 2026-03-19 |
| 00840277405609 - LigaMend™ (Black) | 2026-03-27 Adjustable Loop |
| 00840277405616 - LigaMend™ (Blue) | 2026-03-27 Adjustable Loop |
| 00840277405623 - LigaMend™ | 2026-03-27 Titanium Button |
| 00840277405630 - Strut Suture | 2026-03-27Adjustable Loop |
| 00840277405630 - Strut Suture | 2026-03-27 Adjustable Loop |
| 00840277405715 - LigaMend™ Soft Button (Black) | 2026-03-27 Adjustable Loop |
| 00840277405722 - LigaMend™ Soft Button (Blue) | 2026-03-27 Adjustable Loop |
| 00840277411358 - No-Tie Button | 2026-03-27 Titanium Button |
| 10810020085218 - HS Fiber | 2026-03-24 Suture |