| Primary Device ID | 08809595976781 |
| NIH Device Record Key | 96ff0e0a-bee7-4da3-8f36-894486432d27 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Surgical Instrument |
| Version Model Number | Y1F.45020 |
| Company DUNS | 688999370 |
| Company Name | OSTEONIC CO.,Ltd. |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08809595976781 [Primary] |
| LXH | Orthopedic Manual Surgical Instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[08809595976781]
Moist Heat or Steam Sterilization
[08809595976781]
Moist Heat or Steam Sterilization
[08809595976781]
Moist Heat or Steam Sterilization
[08809595976781]
Moist Heat or Steam Sterilization
[08809595976781]
Moist Heat or Steam Sterilization
[08809595976781]
Moist Heat or Steam Sterilization
[08809595976781]
Moist Heat or Steam Sterilization
[08809595976781]
Moist Heat or Steam Sterilization
[08809595976781]
Moist Heat or Steam Sterilization
[08809595976781]
Moist Heat or Steam Sterilization
[08809595976781]
Moist Heat or Steam Sterilization
[08809595976781]
Moist Heat or Steam Sterilization
[08809595976781]
Moist Heat or Steam Sterilization
[08809595976781]
Moist Heat or Steam Sterilization
[08809595976781]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-07-07 |
| Device Publish Date | 2025-06-27 |