EzDent-i 3.4
EzDent-i 3.4 is a medical device (FDA Class II; FDA product code LLZ, System, Image Processing, Radiological) made by Ewoosoft Co., Ltd., cleared under FDA 510(k) K223820 on 17 Feb 2023 and listed in FDA GUDID since 7 Mar 2023 (UDI-DI 08800019700388), 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 | Number08800019700388 | Date7 Mar 2023 | StatusListed |
| United States | FDA 510(k)SESE | NumberK223820 | Date17 Feb 2023 | StatusActive |
Official records
- AccessGUDID record 08800019700388
- FDA 510(k) database K223820
Across registries
- FDA 510(k) K223820 decided 17 Feb 2023 Active
- FDA GUDID UDI-DI 08800019700388 listed 7 Mar 2023 Listed
Timeline
- Cleared FDA 510(k) K223820
- Listed FDA GUDID 08800019700388
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- EzDent-i
- Generic name
- General-purpose dental x-ray system application software
- Model / reference
- 3.4
- Primary DI / UDI-DI
- 08800019700388
- 510(k) Number
- FDA product code
- LLZ
- GMDN term
- General-purpose dental x-ray system application software
- Device class
- Class II
- Regulation number
- 892.2050
- GUDID distribution status
- In Commercial Distribution