| Primary Device ID | 10886705032525 |
| NIH Device Record Key | 687a23b6-37f9-42a6-9389-9d61472d3d9a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | GRYPHON Flex |
| Version Model Number | 208953 |
| Catalog Number | 208953 |
| Company DUNS | 482661753 |
| Company Name | Medos International Sàrl |
| 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 | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| 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 | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10886705032525 [Primary] |
| FZX | Guide, surgical, instrument |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-05-27 |
| Device Publish Date | 2024-05-17 |
| 10886705032846 | GRYPHON Flex Knotless Anchor Hard Bone Drill [Disposable] |
| 10886705032532 | GRYPHON Flex Knotless Anchor Straight Drill |
| 10886705032525 | GRYPHON Flex Knotless Anchor Sawtooth Straight Guide |
| 10886705032518 | GRYPHON Flex Knotless Anchor Sawtooth Curved Guide |
| 10886705032501 | GRYPHON Flex Knotless Anchor Curved Drill [Disposable] |
| 10886705032488 | GRYPHON Flex Knotless PEEK Anchor PEEK Anchor STRAIGHT |
| 10886705032464 | GRYPHON Flex Knotless Anchor Obturator |
| 10886705032457 | GRYPHON Flex Knotless Anchor Fishmouth Straight Guide |
| 10886705032440 | GRYPHON Flex Knotless Anchor Fishmouth Curved Guide |
| 10886705032433 | GRYPHON Flex Knotless Biocomposite Anchor TCP/PLLA Anchor STRAIGHT |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() GRYPHON FLEX 90501667 not registered Live/Pending |
Johnson & Johnson 2021-02-01 |