| Primary Device ID | 07290110723972 |
| NIH Device Record Key | b35a96a7-c724-425a-9550-069aa388dceb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SELF THREAD /LOGIC PLUS/SPARK |
| Version Model Number | ACA-S |
| Catalog Number | ACA-S |
| Company DUNS | 600710917 |
| Company Name | HI-TEC IMPLANTS LTD. |
| 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 | 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 | 07290110723972 [Primary] |
| NHA | Abutment, Implant, Dental, Endosseous |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-11-08 |
| Device Publish Date | 2017-06-08 |
| 07290110728564 | ABUTMENT SCREW |
| 07290110728557 | ABUTMENT SCREW |
| 07290110728540 | TRANSFER SCREW |
| 07290110728533 | TRANSFER SCREW |
| 07290110728526 | ABUTMENT SCREW |
| 07290110728519 | ABUTMENT SCREW |
| 07290110728502 | ABUTMENT SCREW |
| 07290110723996 | ANTI-ROTATION ABUTMENT |
| 07290110723989 | ANTI-ROTATION ABUTMENT |
| 07290110723972 | ANTI-ROTATION ABUTMENT |
| 07290110723965 | ANTI-ROTATION ABUTMENT |
| 07290110723958 | ANTI-ROTATION ABUTMENT |
| 07290110723941 | ANTI-ROTATION ABUTMENT |
| 07290110723934 | ANTI-ROTATION ABUTMENT |
| 07290110723927 | ANTI-ROTATION ABUTMENT |