| Primary Device ID | 10810113575398 |
| NIH Device Record Key | d90f02b9-570a-417b-b024-e9ba48a34d77 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cyrogrid |
| Version Model Number | SUP3050 |
| Company DUNS | 047025993 |
| Company Name | VIVE HEALTH LLC |
| Device Count | 1 |
| DM Exempt | true |
| 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 | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810113575391 [Primary] |
| GS1 | 10810113575398 [Package] Contains: 00810113575391 Package: Case [6 Units] In Commercial Distribution |
| ITQ | Joint, Knee, External Brace |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-01-19 |
| Device Publish Date | 2024-01-11 |
| 00810113579665 - Vive | 2026-02-17 Hinged Knee Brace (Beige) Medium |
| 00810113579672 - Vive | 2026-02-17 Hinged Knee Brace (Beige) Large |
| 00810113579689 - Vive | 2026-02-17 Hinged Knee Brace (Grey) Medium |
| 00810113579696 - Vive | 2026-02-17 Hinged Knee Brace (Grey) Large |
| 00810178881994 - CoreTech | 2026-02-17 Quick Lace Wrist Brace |
| 00810178882007 - CoreTech | 2026-02-17 Quick Lace Wrist Brace 10" |
| 00810178882533 - CoreTech | 2026-02-17 626 Essential LSO |
| 00810178883219 - Vive | 2026-02-17 Plantar Fasciitis Stretch Splint (Small) |