SonoScape L3-11
SonoScape L3-11 is a Class II device made by Sonoscape Medical Corp., cleared under FDA 510(k) K241949 on 17 Jan 2025 and listed in FDA GUDID since 2 Apr 2025 (UDI-DI 06945868609146), 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 | Number06945868609146 | Date2 Apr 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK241949 | Date17 Jan 2025 | StatusActive |
Official records
- AccessGUDID record 06945868609146
- FDA 510(k) database K241949
Across registries
- FDA 510(k) K241949 decided 17 Jan 2025 Active
- FDA GUDID UDI-DI 06945868609146 listed 2 Apr 2025 Listed
Timeline
- Cleared FDA 510(k) K241949
- Listed FDA GUDID 06945868609146
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- SonoScape
- Generic name
- Extracorporeal ultrasound imaging transducer, hand-held
- Model / reference
- L3-11
- Primary DI / UDI-DI
- 06945868609146
- 510(k) Number
- FDA product code
- ITX, IYO, IYN
- GMDN term
- Extracorporeal ultrasound imaging transducer, hand-held
- Device class
- Class II
- Regulation number
- 892.1570, 892.1560, 892.1550
- GUDID distribution status
- In Commercial Distribution
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