| Primary Device ID | 08415491020598 |
| NIH Device Record Key | c1790a28-f6cc-4703-b701-5972ae814805 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Stern Root Anchor® Standard FG Diamond Bur |
| Version Model Number | 833110 |
| 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 | false |
| 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 | 08415491020598 [Primary] |
| NHA | Abutment, Implant, Dental, Endosseous |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[08415491020598]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-11-08 |
| Device Publish Date | 2017-05-15 |
| 08415491020598 | The Stern Root AnchorSystem includes the Stern Anchor Female (Standard, Mini and casting), The S |
| 00841549106767 | The Stern Root AnchorSystem includes the Stern Anchor Female (Standard, Mini and casting), The S |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() STERN ROOT ANCHOR 85352302 4151629 Live/Registered |
STERNGOLD DENTAL LLC 2011-06-21 |