| Primary Device ID | 10850012846601 |
| NIH Device Record Key | b3342186-2a26-4fe9-952b-964758ff0d5f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | COR-KNOT MESO |
| Version Model Number | 032845 |
| Catalog Number | 032845 |
| Company DUNS | 603420183 |
| Company Name | LSI Solutions, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| 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 | true |
| 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 | 00850012846604 [Primary] |
| GS1 | 10850012846601 [Package] Contains: 00850012846604 Package: Carton [1 Units] In Commercial Distribution |
| GCJ | Laparoscope, general & plastic surgery |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-03-03 |
| Device Publish Date | 2026-02-23 |
| 10850012846618 | COR-KNOT MESO XL Device Twin Pack |
| 10850012846601 | COR-KNOT MESO XL Device |