LW Angled Abutment LWAA60417FHAS
LW Angled Abutment LWAA60417FHAS is a Class II device made by Ossvis Co., Ltd., cleared under FDA 510(k) K233167 on 25 Mar 2024 and listed in FDA GUDID since 21 May 2024 (UDI-DI 08809918223066), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number08809918223066 | Date21 May 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK233167 | Date25 Mar 2024 | StatusActive |
Official records
- AccessGUDID record 08809918223066
- FDA 510(k) database K233167
Across registries
- FDA 510(k) K233167 decided 25 Mar 2024 Active
- FDA GUDID UDI-DI 08809918223066 listed 21 May 2024 Listed
Timeline
- Cleared FDA 510(k) K233167
- Listed FDA GUDID 08809918223066
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- LW Angled Abutment
- Generic name
- Screw endosteal dental implant, two-piece
- Model / reference
- LWAA60417FHAS
- Primary DI / UDI-DI
- 08809918223066
- 510(k) Number
- FDA product code
- NHA
- GMDN term
- Screw endosteal dental implant, two-piece
- 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