| Primary Device ID | 00810125999727 |
| NIH Device Record Key | f1723f17-23cf-4106-b3f8-9329108cc31a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ET STUD ABUTMENT |
| Version Model Number | ETSAO352M |
| Company DUNS | 796083090 |
| Company Name | HIOSSEN, 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 | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810125999727 [Primary] |
| NHA | Abutment, Implant, Dental, Endosseous |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-12-31 |
| Device Publish Date | 2024-12-23 |
| 00810125995514 | ETSA3560C |
| 00810125995507 | ETSA3550C |
| 00810125995491 | ETSA3540C |
| 00810125995484 | ETSA3530C |
| 00810125995477 | ETSA3520C |
| 00810125995460 | ETSA3510C |
| 00810125995453 | ETSAM3560C |
| 00810125995446 | ETSAM3550C |
| 00810125995439 | ETSAM3540C |
| 00810125995422 | ETSAM3530C |
| 00810125995415 | ETSAM3520C |
| 00810125995408 | ETSAM3510C |
| 00810125999819 | ETSAO356S |
| 00810125999802 | ETSAO356M |
| 00810125999796 | ETSAO355S |
| 00810125999789 | ETSAO355M |
| 00810125999772 | ETSAO354S |
| 00810125999765 | ETSAO354M |
| 00810125999758 | ETSAO353S |
| 00810125999741 | ETSAO353M |
| 00810125999734 | ETSAO352S |
| 00810125999727 | ETSAO352M |
| 00810125999710 | ETSAO351S |
| 00810125999703 | ETSAO351M |