| Primary Device ID | 00810008462034 |
| NIH Device Record Key | 7efc4fc4-46d1-4559-b986-e20eba7b44b5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Abutment |
| Version Model Number | RRSA04 |
| Company DUNS | 050003777 |
| Company Name | Little Implant Co. |
| Device Count | 1 |
| DM Exempt | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810008462034 [Primary] |
| NHA | Abutment, Implant, Dental, Endosseous |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00810008462034]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-11-08 |
| Device Publish Date | 2019-05-13 |
| 00810008462508 | Screw for Abutment |
| 00810008462317 | 15° Abutment - Length 9mm |
| 00810008462041 | THE TONY FECK™ Straight Abutment-ht 0.5 |
| 00810008462034 | THE TONY FECK™ Straight Abutment-ht 4.5 |
| 00810008462027 | THE TONY FECK™ Straight Abutment-ht 2.5 |
| 00810008462669 | THE TONY FECK™ Non-rotational Temporary Abutment |
| 00810008462607 | PEEK Temporary Abutment 3mm |
| 00810008462591 | PEEK Temporary Abutment 2mm |
| 00810008462584 | PEEK Temporary Abutment 1mm |