| Primary Device ID | 00810056990534 |
| NIH Device Record Key | 84953495-d38d-4905-ab00-f271bedf2a54 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | aprevo |
| Version Model Number | G.L23.03 |
| Company DUNS | 117449452 |
| Company Name | Carlsmed, Inc. |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810056990534 [Primary] |
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-10-15 |
| Device Publish Date | 2021-10-07 |
| 00810056990756 | aprevo Inserter |
| 00810056990749 | aprevo Rod Bending Template, Right |
| 00810056990732 | aprevo Rod Bending Template, Left |
| 00810056990725 | aprevo LLIF L5/S1, plus |
| 00810056990718 | aprevo LLIF L5/S1, plan |
| 00810056990701 | aprevo LLIF L5/S1, minus |
| 00810056990671 | aprevo LLIF L4/L5, plus |
| 00810056990664 | aprevo LLIF L4/L5, plan |
| 00810056990657 | aprevo LLIF L4/L5, minus |
| 00810056990626 | aprevo LLIF L3/L4, plus |
| 00810056990619 | aprevo LLIF L3/L4, plan |
| 00810056990602 | aprevo LLIF L3/L4, minus |
| 00810056990572 | aprevo LLIF L2/L3, plus |
| 00810056990565 | aprevo LLIF L2/L3, plan |
| 00810056990558 | aprevo LLIF L2/L3, minus |
| 00810056990527 | aprevo LLIF L1/L2, plus |
| 00810056990510 | aprevo LLIF L1/L2, plan |
| 00810056990503 | aprevo LLIF L1/L2, minus |
| 00810056990473 | aprevo A/LLIF L5/S1, plus |
| 00810056990466 | aprevo A/LLIF L5/S1, plan |
| 00810056990459 | aprevo A/LLIF L5/S1, minus |
| 00810056990428 | aprevo A/LLIF L4/L5, plus |
| 00810056990411 | aprevo A/LLIF L4/L5, plan |
| 00810056990404 | aprevo A/LLIF L4/L5, minus |
| 00810056990374 | aprevo A/LLIF L3/L4, plus |
| 00810056990367 | aprevo A/LLIF L3/L4, plan |
| 00810056990350 | aprevo A/LLIF L3/L4, minus |
| 00810056990329 | aprevo A/LLIF L2/L3, plus |
| 00810056990312 | aprevo A/LLIF L2/L3, plan |
| 00810056990305 | aprevo A/LLIF L2/L3, minus |
| 00810056990275 | aprevo A/LLIF L1/L2, plus |
| 00810056990268 | aprevo A/LLIF L1/L2, plan |
| 00810056990251 | aprevo A/LLIF L1/L2, minus |
| 00810056990220 | aprevo ALIF L5/S1, plus |
| 00810056990213 | aprevo ALIF L5/S1, plan |
| 00810056990206 | aprevo ALIF L5/S1, minus |
| 00810056990176 | aprevo ALIF L4/L5, plus |
| 00810056990169 | aprevo ALIF L4/L5, plan |
| 00810056990152 | aprevo ALIF L4/L5, minus |
| 00810056990121 | aprevo ALIF L3/L4, plus |
| 00810056990114 | aprevo ALIF L3/L4, plan |
| 00810056990107 | aprevo ALIF L3/L4, minus |
| 00810056990077 | aprevo ALIF L2/L3, plus |
| 00810056990060 | aprevo ALIF L2/L3, plan |
| 00810056990053 | aprevo ALIF L2/L3, minus |
| 00810056990022 | aprevo ALIF L1/L2, plus |
| 00810056990015 | aprevo ALIF L1/L2, plan |
| 00810056990008 | aprevo ALIF L1/L2, minus |
| 00810056990862 | aprevo TLIF-O L5/S1, plus |
| 00810056990855 | aprevo TLIF-O L5/S1, plan |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() APREVO 97260623 not registered Live/Pending |
Carlsmed, Inc. 2022-02-09 |
![]() APREVO 97260610 not registered Live/Pending |
Carlsmed, Inc. 2022-02-09 |
![]() APREVO 88768306 not registered Live/Pending |
Carlsmed, Inc. 2020-01-21 |