| Primary Device ID | 10841307109716 | 
| NIH Device Record Key | 3b998eb2-541c-4b55-8030-50dca0f9a433 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | InterActive® GPS® Abutment Narrow | 
| Version Model Number | 6530-91N | 
| Catalog Number | 6530-91N | 
| Company DUNS | 868856969 | 
| Company Name | IMPLANT DIRECT SYBRON MANUFACTURING 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 | true | 
| Device Combination Product | false | 
| Single Use | true | 
| 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 | 
| Phone | 1-888-649-6425 | 
| customerservice@implantdirect.com | 
| Device Size Text, specify | 0 | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 10841307109716 [Primary] | 
| NHA | Abutment, Implant, Dental, Endosseous | 
| Steralize Prior To Use | true | 
| Device Is Sterile | false | 
[10841307109716]
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 | 2015-09-14 | 
| 10841307109822 | 6534-96N | 
| 10841307109815 | 6534-95N | 
| 10841307109808 | 6534-94N | 
| 10841307109792 | 6534-93N | 
| 10841307109785 | 6534-92N | 
| 10841307109778 | 6534-91N | 
| 10841307109761 | 6530-96N | 
| 10841307109754 | 6530-95N | 
| 10841307109747 | 6530-94N | 
| 10841307109730 | 6530-93N | 
| 10841307109723 | 6530-92N | 
| 10841307109716 | 6530-91N |