Simplant Version 3.1
by Dentsply Implants NV 2 variants
Simplant Version 3.1 (54500395IV31) is a Class II device made by Dentsply Implants NV, listed in FDA GUDID since 11 Mar 2019 (UDI-DI 07392532209413), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number07392532209413 | Date11 Mar 2019 | StatusListed |
Official records
- AccessGUDID record 07392532209413
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Simplant
- Generic name
- Panoramic/tomographic dental x-ray system application software
- Model / Ref / Catalog
- Version 3.1, 54500395IV31
- Primary DI / UDI-DI
- 07392532209413
- FDA product code
- LLZ
- GMDN term
- Panoramic/tomographic dental x-ray system application software
- Device class
- Class II
- Regulation number
- 892.2050
- GUDID distribution status
- In Commercial Distribution
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