Xtg V 1
Xtg V 1 is a hand-held intraoral dental x-ray system (FDA Class II; FDA product code EHD, Unit, X-Ray, Extraoral With Timer) made by DigiMed Co., Ltd., cleared under FDA 510(k) K181891 on 10 Aug 2018 and listed in FDA GUDID since 1 Jun 2026 (UDI-DI 08800021800175), active as of 12 Nov 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 | Number08800021800175 | Date1 Jun 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK181891 | Date10 Aug 2018 | StatusActive |
Official records
- AccessGUDID record 08800021800175
- FDA 510(k) database K181891
Across registries
- FDA 510(k) K181891 decided 10 Aug 2018 Active
- FDA GUDID UDI-DI 08800021800175 listed 1 Jun 2026 Listed
Timeline
- Cleared FDA 510(k) K181891
- Listed FDA GUDID 08800021800175
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Xtg V
- Generic name
- Hand-held intraoral dental x-ray system, digital
- Model / Ref / Catalog
- 1
- Primary DI / UDI-DI
- 08800021800175
- 510(k) Number
- FDA product code
- EHD
- GMDN term
- Hand-held intraoral dental x-ray system, digital
- Device class
- Class II
- Regulation number
- 872.1800
- GUDID distribution status
- In Commercial Distribution
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