| Primary Device ID | 00859070006050 |
| NIH Device Record Key | 03dd2c84-d860-4a42-a3d1-4397018cda56 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LipoGrafter |
| Version Model Number | 913000 |
| Company DUNS | 187560545 |
| Company Name | Musculoskeletal Transplant Foundation, Inc. |
| 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 | true |
| 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 |
| Phone | 800-433-6576 |
| RA_Licenses@mtf.org |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00859070006050 [Primary] |
| KYZ | Syringe, Irrigating (Non Dental) |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-10-22 |
| Device Publish Date | 2018-09-21 |
| W4184420800T0473 - Legacy DBM | 2022-07-11 Legacy DBM, 0.5cc |
| W4184420801T0473 - Legacy DBM | 2022-07-11 Legacy DBM, 1CC |
| W4184420802T0473 - Legacy DBM | 2022-07-11 Legacy DBM, 2.5CC |
| W4184420805T0473 - Legacy DBM | 2022-07-11 Legacy DBM, 5CC |
| W4184048010T0479 - DBX® | 2019-06-13 DBX Strip 2.5cm x 10cm |
| W4184048015T0479 - DBX® | 2019-06-13 DBX Strip 1.5cm x 1.5cm |
| W4184048025T0479 - DBX® | 2019-06-13 DBX Strip 2.5cm x 5cm |
| W4184048050T0479 - DBX® | 2019-06-13 DBX Strip 5cm x 5cm |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LIPOGRAFTER 77934879 3967300 Live/Registered |
Lipocosm, LLC 2010-02-12 |