| Primary Device ID | 07290110721756 |
| NIH Device Record Key | 06ab323e-592c-41f4-a452-f508642b7abb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TAPERED TITE FIT |
| Version Model Number | TFR-16mm |
| Catalog Number | TFR-16 |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07290110721756 [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 |
| 07290110721800 | DENTAL IMPLANT |
| 07290110721794 | DENTAL IMPLANT |
| 07290110721787 | DENTAL IMPLANT |
| 07290110721770 | DENTAL IMPLANT |
| 07290110721763 | DENTAL IMPLANT |
| 07290110721756 | DENTAL IMPLANT |
| 07290110721749 | DENTAL IMPLANT |
| 07290110721732 | DENTAL IMPLANT |
| 07290110721725 | DENTAL IMPLANT |
| 07290110721718 | DENTAL IMPLANT |
| 07290110721701 | DENTAL IMPLANT |
| 07290110721695 | DENTAL IMPLANT |
| 07290110721688 | DENTAL IMPLANT |
| 07290110721671 | DENTAL IMPLANT |
| 07290110721664 | DENTAL IMPLANT |