| Primary Device ID | 00810126041371 |
| NIH Device Record Key | 718b45e8-a6b4-4ecd-a2a0-51270cf6229f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EK Pre-milled Abutment |
| Version Model Number | EKPMA14CANT |
| Company DUNS | 796083090 |
| Company Name | HIOSSEN, INC. |
| 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 | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810126041371 [Primary] |
| NHA | Abutment, Implant, Dental, Endosseous |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-02-25 |
| Device Publish Date | 2025-02-17 |
| 00810126041418 | EKPMA14ZKNT |
| 00810126041401 | EKPMA14ZKHT |
| 00810126041395 | EKPMA14MXNT |
| 00810126041388 | EKPMA14MXHT |
| 00810126041371 | EKPMA14CANT |
| 00810126041364 | EKPMA14CAHT |
| 00810126041357 | EKPMA14ARNT |
| 00810126041340 | EKPMA14ARHT |
| 00810126041333 | EKPMA14ANNT |
| 00810126041326 | EKPMA14ANHT |
| 00810126041319 | EKPMA12CENT |
| 00810126041302 | EKPMA12CEHT |
| 00810126041296 | EKPMA10ZKNT |
| 00810126041289 | EKPMA10ZKHT |
| 00810126041272 | EKPMA10MXNT |
| 00810126041265 | EKPMA10MXHT |
| 00810126041258 | EKPMA10CANT |
| 00810126041241 | EKPMA10CAHT |
| 00810126041234 | EKPMA10ARNT |
| 00810126041227 | EKPMA10ARHT |
| 00810126041210 | EKPMA10ANNT |
| 00810126041203 | EKPMA10ANHT |
| 00810126041104 | ETPMA14CARHW |