Senolo XE23
by Jiangsu Senolo Medical Technology Co., Ltd.
Senolo XE23 is a Class I device made by Jiangsu Senolo Medical Technology Co., Ltd., listed in FDA GUDID since 6 Apr 2023 (UDI-DI 26952534451026), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number26952534451026 | Date6 Apr 2023 | StatusListed |
Official records
- AccessGUDID record 26952534451026
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Senolo
- Generic name
- Cast construction material
- Model / reference
- XE23
- Primary DI / UDI-DI
- 26952534451026
- FDA product code
- ITG
- GMDN term
- Cast construction material
- Device class
- Class I
- Regulation number
- 890.3025
- GUDID distribution status
- In Commercial Distribution
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