| Primary Device ID | 30653405990721 |
| NIH Device Record Key | a4a41cef-5c91-46a8-bd89-14e4959da11f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Y-KnotlessTM Flex |
| Version Model Number | YKF-W |
| Catalog Number | YKF-W |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| 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 |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 20653405990724 [Primary] |
| GS1 | 30653405990721 [Package] Contains: 20653405990724 Package: Carton [1 Units] In Commercial Distribution |
| MBI | Fastener, fixation, nondegradable, soft tissue |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-02-16 |
| Device Publish Date | 2026-02-06 |
| 30653405990721 | Y-KnotlessTM Flex Anchor, White/Black #2 Hi-Fi Suture, 1.8 mm |
| 30653405546508 | Y-KnotlessTM Flex Anchor, Green/Black #2 Hi-Fi Suture, 1.8 mm |