| Primary Device ID | 08435452017306 |
| NIH Device Record Key | e8c9c4ba-a034-4bf3-ab85-31d8c30be47c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AVINENT |
| Version Model Number | 4805 |
| Company DUNS | 477451012 |
| Company Name | AVINENT IMPLANT SYSTEM SLU |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| 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 | 08435452017306 [Primary] |
| NDP | Accessories, implant, dental, endosseous |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[08435452017306]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-09-23 |
| Device Publish Date | 2019-09-13 |
| 08435452018488 | Scan Analog Prima PlusTM Ø5,0 CORE3D |
| 08435452018471 | Scan Analog Prima PlusTM Ø4,1 CORE3D |
| 08435452018464 | Scan Analog Prima PlusTM Ø3,5 CORE3D |
| 08435452018457 | Scan Analog Genesis Ø3,5 CORE3D |
| 08435452018440 | Scan Analog Prima PlusTM Ø6,0 CORE3D |
| 08435452018358 | Scan Analog TILOBEMAXXTM Ø8,0 CORE3D |
| 08435452018341 | Scan Analog TILOBEMAXXTM Ø7,0 CORE3D |
| 08435452018334 | Scan Analog Genesis Ø6,5 CORE3D |
| 08435452018327 | Scan Analog Genesis Ø5,5 CORE3D |
| 08435452018310 | Scan Analog Genesis Ø4,5 CORE3D |
| 08435452018303 | Scan Analog Genesis Ø3,8 CORE3D |
| 08435452018297 | Scan Analog PrimaConnex® Ø5,0 CORE3D |
| 08435452018280 | Scan Analog PrimaConnex® Ø4,1 CORE3D |
| 08435452018273 | Scan Analog PrimaConnex® Ø3,5 CORE3D |
| 08435452017405 | Scan Abutment Prima PlusTM Ø6,0 CORE3D |
| 08435452017399 | Scan Abutment Prima PlusTM Ø5,0 CORE3D |
| 08435452017382 | Scan Abutment Prima PlusTM Ø4,1 CORE3D |
| 08435452017375 | Scan Abutment Prima PlusTM Ø3,5 CORE3D |
| 08435452017368 | Scan Abutment TILOBEMAXXTM Ø8,0 CORE3D |
| 08435452017351 | Scan Abutment TILOBEMAXXTM Ø7,0 CORE3D |
| 08435452017344 | Scan Abutment Genesis Ø6,5 CORE3D |
| 08435452017337 | Scan Abutment Genesis Ø5,5 CORE3D |
| 08435452017320 | Scan Abutment Genesis Ø4,5 CORE3D |
| 08435452017313 | Scan Abutment Genesis Ø3,8 CORE3D |
| 08435452017306 | Scan Abutment Genesis Ø3,5 CORE3D |
| 08435452017290 | Scan Abutment PrimaConnex® Ø5,0 CORE3D |
| 08435452017283 | Scan Abutment PrimaConnex® Ø4,1 CORE3D |
| 08435452017276 | Scan Abutment PrimaConnex® Ø3,5 CORE3D |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() AVINENT 88424146 not registered Live/Pending |
Avinent Implant System, S.L. 2019-05-10 |
![]() AVINENT 86246511 not registered Live/Pending |
Avinent Canada Ltd. 2014-04-08 |