| Primary Device ID | 00810125994142 |
| NIH Device Record Key | 2a1594dd-3422-451a-9ec9-a7d00262fe9b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ET FREEFORM ST ABUTMENT SET |
| Version Model Number | ETFAM4015NCWH |
| 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 | 00810125994142 [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 | 2024-07-15 |
| Device Publish Date | 2024-07-06 |
| 00810125994364 | ETFAS5030NCWH |
| 00810125994357 | ETFAS5030CWH |
| 00810125994340 | ETFAS5015NCWH |
| 00810125994333 | ETFAS5015CWH |
| 00810125994326 | ETFA7030NCWH |
| 00810125994319 | ETFA7030CWH |
| 00810125994302 | ETFA7015NCWH |
| 00810125994296 | ETFA7015CWH |
| 00810125994289 | ETFA6030NCWH |
| 00810125994272 | ETFA6030CWH |
| 00810125994265 | ETFA6015NCWH |
| 00810125994258 | ETFA6015CWH |
| 00810125994241 | ETFA5030NCWH |
| 00810125994234 | ETFA5030CWH |
| 00810125994227 | ETFA5015NCWH |
| 00810125994210 | ETFA5015CWH |
| 00810125994203 | ETFA4030NCWH |
| 00810125994197 | ETFA4030CWH |
| 00810125994180 | ETFA4015NCWH |
| 00810125994173 | ETFA4015CWH |
| 00810125994166 | ETFAM4030NCWH |
| 00810125994159 | ETFAM4030CWH |
| 00810125994142 | ETFAM4015NCWH |
| 00810125994135 | ETFAM4015CWH |