| Primary Device ID | 07290105150417 |
| NIH Device Record Key | 6722ae28-e104-494e-bb89-0772e3788924 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Swell™ Dental Implant 4.2D 6.25L |
| Version Model Number | ID0642 |
| Company DUNS | 533289435 |
| Company Name | ADIN DENTAL IMPLANT SYSTEMS LTD |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07290105150417 [Primary] |
| DZE | Implant, Endosseous, Root-Form |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-07-25 |
| Device Publish Date | 2022-07-17 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
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Timbuk2 Designs, Inc. 2022-05-04 |
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Revolution Boards LLC 2021-05-06 |
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Central Pacific Bank 2020-12-09 |