Implant Prosthetics 8000362
Implant Prosthetics 8000362 is a Class II device made by PREAT Corporation, listed in FDA GUDID since 16 Sep 2016 (UDI-DI 00842092117095), registry data as of 22 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 | Number00842092117095 | Date16 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00842092117095
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Implant Prosthetics
- Generic name
- Dental implant suprastructure, permanent, preformed
- Model / Ref / Catalog
- 8000362
- Primary DI / UDI-DI
- 00842092117095
- FDA product code
- NHA
- GMDN term
- Dental implant suprastructure, permanent, preformed
- Device class
- Class II
- Regulation number
- 872.3630
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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