Cemented Abutment OSCA5042HP
Cemented Abutment OSCA5042HP is a Class II device made by POINTIMPLANT Co., Ltd., listed in FDA GUDID since 13 Feb 2025 (UDI-DI 08800011237783), 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 | Number08800011237783 | Date13 Feb 2025 | StatusListed |
Official records
- AccessGUDID record 08800011237783
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Cemented Abutment
- Generic name
- Dental implant suprastructure, permanent, preformed
- Model / reference
- OSCA5042HP
- Primary DI / UDI-DI
- 08800011237783
- 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
- MRI safety
- MR Conditional
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