LUNA 3D Central Server Software
by L a P GmbH Laser Applikationen
LUNA 3D Central Server Software (0018440) is a Class II device made by L a P GmbH Laser Applikationen, cleared under FDA 510(k) K232031 on 29 Mar 2024 and listed in FDA GUDID since 17 Jun 2024 (UDI-DI 04260590372673), 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 | Number04260590372673 | Date17 Jun 2024 | StatusListed |
| United States | FDA 510(k) | NumberK232031 | Date29 Mar 2024 | StatusActive |
Official records
- AccessGUDID record 04260590372673
- FDA 510(k) database K232031
Across registries
- FDA 510(k) K232031 decided 29 Mar 2024 Active
- FDA GUDID UDI-DI 04260590372673 listed 17 Jun 2024 Listed
Timeline
- Cleared FDA 510(k) K232031
- Listed FDA GUDID 04260590372673
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Luna 3D
- Generic name
- Radiological video camera patient positioning/tracking system
- Model / Ref / Catalog
- LUNA 3D Central Server Software, 0018440
- Primary DI / UDI-DI
- 04260590372673
- 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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