| Primary Device ID | 00810019240775 |
| NIH Device Record Key | c36b6734-713f-4d00-837c-65097221cdaf |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ET FREEFORM ST ABUTMENT |
| Version Model Number | ETFSA403MHW |
| 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 | 00810019240775 [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 | 2019-05-23 |
| Device Publish Date | 2019-05-15 |
| 00810019240980 | ETFSA703SNW |
| 00810019240973 | ETFSA703SHW |
| 00810019240966 | ETFSA701SNW |
| 00810019240959 | ETFSA701SHW |
| 00810019240942 | ETFSA603SNW |
| 00810019240935 | ETFSA603SHW |
| 00810019240928 | ETFSA601SNW |
| 00810019240911 | ETFSA601SHW |
| 00810019240904 | ETFSA503SNW |
| 00810019240898 | ETFSA503SHW |
| 00810019240881 | ETFSA501SNW |
| 00810019240874 | ETFSA501SHW |
| 00810019240867 | ETFSAS503SNW |
| 00810019240850 | ETFSAS503SHW |
| 00810019240843 | ETFSAS501SNW |
| 00810019240836 | ETFSAS501SHW |
| 00810019240829 | ETFSA403SNW |
| 00810019240812 | ETFSA403SHW |
| 00810019240805 | ETFSA401SNW |
| 00810019240799 | ETFSA401SHW |
| 00810019240782 | ETFSA403MNW |
| 00810019240775 | ETFSA403MHW |
| 00810019240768 | ETFSA401MNW |
| 00810019240751 | ETFSA401MHW |