AlignRT Plus Touchless4D
AlignRT Plus Touchless4D is a Class II device made by Vision RT Limited, cleared under FDA 510(k) K212583 on 10 Nov 2021 and listed in FDA GUDID since 9 Dec 2021 (UDI-DI 05056190500672), active as of 22 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 | Number05056190500672 | Date9 Dec 2021 | StatusListed |
| United States | FDA 510(k) | NumberK212583 | Date10 Nov 2021 | StatusActive |
Official records
- AccessGUDID record 05056190500672
- FDA 510(k) database K212583
Across registries
- FDA 510(k) K212583 decided 10 Nov 2021 Active
- FDA GUDID UDI-DI 05056190500672 listed 9 Dec 2021 Listed
Timeline
- Cleared FDA 510(k) K212583
- Listed FDA GUDID 05056190500672
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- AlignRT Plus
- Generic name
- Radiological video camera patient positioning/tracking system
- Model / reference
- Touchless4D
- Primary DI / UDI-DI
- 05056190500672
- 510(k) Number
- FDA product code
- IYE
- GMDN term
- Radiological video camera patient positioning/tracking system
- Device class
- Class II
- Regulation number
- 892.5050
- GUDID distribution status
- In Commercial Distribution
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