| Primary Device ID | 08415491043450 |
| NIH Device Record Key | ac36e381-42ff-4b8a-9b3a-e9ff55a42f53 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Natural Profile Healing Abutment |
| Version Model Number | 904263 |
| Company DUNS | 124763728 |
| Company Name | STERNGOLD DENTAL LLC |
| 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 |
| Phone | 401-871-3489 |
| maria.rao@sterngold.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08415491043450 [Primary] |
| DZE | Implant, Endosseous, Root-Form |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-11-08 |
| Device Publish Date | 2016-10-10 |
| 08415491043450 | Devices are used in dental implant applications for oral rehabilitation of edentulous and partia |
| 08415491039750 | Devices are used in dental implant applications for oral rehabilitation of edentulous and partia |
| 08415491016003 | Devices are used in dental implant applications for oral rehabilitation of edentulous and partia |
| 00841549111716 | Devices are used in dental implant applications for oral rehabilitation of edentulous and partia |
| 00841549110832 | Devices are used in dental implant applications for oral rehabilitation of edentulous and partia |
| 00841549110733 | Devices are used in dental implant applications for oral rehabilitation of edentulous and partia |