LW Solid Abutment LWSA6024F
LW Solid Abutment LWSA6024F is a Class II device made by Ossvis Co., Ltd., cleared under FDA 510(k) K223924 on 8 Aug 2023 and listed in FDA GUDID since 18 Dec 2023 (UDI-DI 08809918210875), 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 | Number08809918210875 | Date18 Dec 2023 | StatusListed |
| United States | FDA 510(k)SESE | NumberK223924 | Date8 Aug 2023 | StatusActive |
Official records
- AccessGUDID record 08809918210875
- FDA 510(k) database K223924
Across registries
- FDA 510(k) K223924 decided 8 Aug 2023 Active
- FDA GUDID UDI-DI 08809918210875 listed 18 Dec 2023 Listed
Timeline
- Cleared FDA 510(k) K223924
- Listed FDA GUDID 08809918210875
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- LW Solid Abutment
- Generic name
- Screw endosteal dental implant, two-piece
- Model / reference
- LWSA6024F
- Primary DI / UDI-DI
- 08809918210875
- 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
- MRI safety
- MR Conditional
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