EzDent-i v2.3
EzDent-i v2.3 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) K172364 on 22 Aug 2017 and listed in FDA GUDID since 1 Sep 2017 (UDI-DI 08800019700074), 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 | Number08800019700074 | Date1 Sep 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK172364 | Date22 Aug 2017 | StatusActive |
Official records
- AccessGUDID record 08800019700074
- FDA 510(k) database K172364
Across registries
- FDA 510(k) K172364 decided 22 Aug 2017 Active
- FDA GUDID UDI-DI 08800019700074 listed 1 Sep 2017 Listed
Timeline
- Cleared FDA 510(k) K172364
- Listed FDA GUDID 08800019700074
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- Withdrawn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
- v2.3
- Primary DI / UDI-DI
- 08800019700074
- 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