| Primary Device ID | 07290110720100 |
| NIH Device Record Key | 021fca4f-63e3-45b0-a9de-927072714d61 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TAPERED SELF THREAD |
| Version Model Number | SLT-16mmSR |
| Catalog Number | SLT-16SR |
| 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 | true |
| 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 | 07290110720100 [Primary] |
| NHA | Abutment, Implant, Dental, Endosseous |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2017-05-22 |
| 07290110720209 | DENTAL IMPLANT |
| 07290110720193 | DENTAL IMPLANT |
| 07290110720186 | DENTAL IMPLANT |
| 07290110720179 | DENTAL IMPLANT |
| 07290110720162 | DENTAL IMPLANT |
| 07290110720155 | DENTAL IMPLANT |
| 07290110720148 | DENTAL IMPLANT |
| 07290110720131 | DENTAL IMPLANT |
| 07290110720124 | DENTAL IMPLANT |
| 07290110720117 | DENTAL IMPLANT |
| 07290110720100 | DENTAL IMPLANT |
| 07290110720094 | DENTAL IMPLANT |
| 07290110720087 | DENTAL IMPLANT |
| 07290110720070 | DENTAL IMPLANT |
| 07290110720063 | SLT-8mmSR |
| 07290110720056 | NTI-16mmSR |
| 07290110720049 | NTI-13mmSR |
| 07290110720032 | NTI-11.5mmSR |
| 07290110720025 | NTI-10mmSR |
| 07290110720018 | NTI-8mmSR |