REX IMPLANTS
GUDID 08435673513939
Dynamic TiBase R G0.6 Comp.0040
TALLADIUM ESPAÑA SL
Dental implant suprastructure, permanent, preformed| Primary Device ID | 08435673513939 |
| NIH Device Record Key | 5830c5bf-75da-4e80-8f0e-9052d7c6dce5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | REX IMPLANTS |
| Version Model Number | 31.322.040.01-2H |
| Company DUNS | 510591266 |
| Company Name | TALLADIUM ESPAÑA SL |
| 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 |
Customer Support Contacts
| Phone | +34973289580 |
| das@dynamicabutment.com | |
| Phone | +34973289580 |
| das@dynamicabutment.com | |
| Phone | +34973289580 |
| das@dynamicabutment.com | |
| Phone | +34973289580 |
| das@dynamicabutment.com | |
| Phone | +34973289580 |
| das@dynamicabutment.com | |
| Phone | +34973289580 |
| das@dynamicabutment.com | |
| Phone | +34973289580 |
| das@dynamicabutment.com | |
| Phone | +34973289580 |
| das@dynamicabutment.com | |
| Phone | +34973289580 |
| das@dynamicabutment.com | |
| Phone | +34973289580 |
| das@dynamicabutment.com | |
| Phone | +34973289580 |
| das@dynamicabutment.com | |
| Phone | +34973289580 |
| das@dynamicabutment.com | |
| Phone | +34973289580 |
| das@dynamicabutment.com | |
| Phone | +34973289580 |
| das@dynamicabutment.com |
Operating and Storage Conditions
| Storage Environment Temperature | Between 18 Degrees Celsius and 25 Degrees Celsius |
| Storage Environment Temperature | Between 18 Degrees Celsius and 25 Degrees Celsius |
| Storage Environment Temperature | Between 18 Degrees Celsius and 25 Degrees Celsius |
| Storage Environment Temperature | Between 18 Degrees Celsius and 25 Degrees Celsius |
| Storage Environment Temperature | Between 18 Degrees Celsius and 25 Degrees Celsius |
| Storage Environment Temperature | Between 18 Degrees Celsius and 25 Degrees Celsius |
| Storage Environment Temperature | Between 18 Degrees Celsius and 25 Degrees Celsius |
| Storage Environment Temperature | Between 18 Degrees Celsius and 25 Degrees Celsius |
| Storage Environment Temperature | Between 18 Degrees Celsius and 25 Degrees Celsius |
| Storage Environment Temperature | Between 18 Degrees Celsius and 25 Degrees Celsius |
| Storage Environment Temperature | Between 18 Degrees Celsius and 25 Degrees Celsius |
| Storage Environment Temperature | Between 18 Degrees Celsius and 25 Degrees Celsius |
| Storage Environment Temperature | Between 18 Degrees Celsius and 25 Degrees Celsius |
| Storage Environment Temperature | Between 18 Degrees Celsius and 25 Degrees Celsius |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08435673513939 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K232151
FDA Product Code
| NHA | Abutment, Implant, Dental, Endosseous |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[08435673513939]
Moist Heat or Steam Sterilization
[08435673513939]
Moist Heat or Steam Sterilization
[08435673513939]
Moist Heat or Steam Sterilization
[08435673513939]
Moist Heat or Steam Sterilization
[08435673513939]
Moist Heat or Steam Sterilization
[08435673513939]
Moist Heat or Steam Sterilization
[08435673513939]
Moist Heat or Steam Sterilization
[08435673513939]
Moist Heat or Steam Sterilization
[08435673513939]
Moist Heat or Steam Sterilization
[08435673513939]
Moist Heat or Steam Sterilization
[08435673513939]
Moist Heat or Steam Sterilization
[08435673513939]
Moist Heat or Steam Sterilization
[08435673513939]
Moist Heat or Steam Sterilization
[08435673513939]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-02-19 |
| Device Publish Date | 2025-02-11 |
On-Brand Devices [REX IMPLANTS]
| 08435673514073 | Dynamic Abutment, NR, POM, 25 Comp.0040 |
| 08435673514066 | Dynamic Abutment, R, POM, 25 Comp.0040 |
| 08435673514059 | Dynamic screwdriver. L32mm 30 |
| 08435673514042 | Dynamic screwdriver. L24mm 30 |
| 08435673514035 | Dynamic screwdriver. L18mm 30 |
| 08435673514028 | Dynamic Screw M1.8 L7.1mm 25N.cm |
| 08435673514011 | Dynamic TiBase R G5 Comp.0040 |
| 08435673514004 | Dynamic TiBase NR G5 Comp.0040 |
| 08435673513991 | Dynamic TiBase R G4 Comp.0040 |
| 08435673513984 | Dynamic TiBase NR G4 Comp.0040 |
| 08435673513977 | Dynamic TiBase R G3 Comp.0040 |
| 08435673513960 | Dynamic TiBase NR G3 Comp.0040 |
| 08435673513953 | Dynamic TiBase NR G1.5 Comp.0040 |
| 08435673513946 | Dynamic TiBase R G1.5 Comp.0040 |
| 08435673513939 | Dynamic TiBase R G0.6 Comp.0040 |
| 08435673513922 | Dynamic TiBase NR G0.6 Comp.0040 |
Trademark Results [REX IMPLANTS]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 REX IMPLANTS 87917437 not registered Dead/Abandoned |
Rex Implants, Inc. 2018-05-11 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.