| Primary Device ID | 00850005827238 |
| NIH Device Record Key | 0001a0da-1129-4769-bca3-bfd5231d0095 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | GENESIS SCREW-IN SUTURE ANCHOR |
| Version Model Number | 10B65003 |
| Catalog Number | 10B65003 |
| Company DUNS | 016463487 |
| Company Name | Genesis Biologics, 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 | 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 | 00850005827238 [Primary] |
| MAI | Fastener, Fixation, Biodegradable, 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 | 2023-03-24 |
| Device Publish Date | 2023-03-16 |
| 00850005827238 | 6.5MM SCREW-IN SUTURE ANCHOR |
| 00850005827221 | 5.5MM SCREW-IN SUTURE ANCHOR |
| 00850005827214 | 4.5MM SCREW-IN SUTURE ANCHOR |