Senolo XE33
by Jiangsu Senolo Medical Technology Co., Ltd.
Senolo XE33 is a Class I device made by Jiangsu Senolo Medical Technology Co., Ltd., listed in FDA GUDID since 6 Apr 2023 (UDI-DI 26952534451033), 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 | Number26952534451033 | Date6 Apr 2023 | StatusListed |
Official records
- AccessGUDID record 26952534451033
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Senolo
- Generic name
- Cast construction material
- Model / reference
- XE33
- Primary DI / UDI-DI
- 26952534451033
- FDA product code
- ITG
- GMDN term
- Cast construction material
- Device class
- Class I
- Regulation number
- 890.3025
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code ITG (Bandage, Cast).
- Webril 3489 by Cardinal Health 200, LLC
- BVN by Donald J. Mangus, M.D.
- Webril 1418 by Cardinal Health 200, LLC
- COTTON UNDER CAST PADDING by Winn Hirsch & Assoc.
- LIGHTCAST II CASTING SYSTEM (MODIFIED) by Solar Laboratories, Inc.
- SOFFBAN ORTHOPEDIC PADDING by Smith & Nephew, Inc.
- 3M ORTHOPEDIC CASTING TAPE by 3M COMPANY
- ULTRACAST WATERLESS SYNTHETIC RESIN CAST by Zimmer, Inc.
- YESONA PLASTER OF PARIS BANDAGE by Watson Phillips Y Cia. Sucs., S.A. DE C.V.
- BANDAGES, PLASTER OF PARIS & SPLINTS by Johnson & Johnson Professionals, Inc.
Other devices from Jiangsu Senolo Medical Technology Co., Ltd.
See all devices from Jiangsu Senolo Medical Technology Co., Ltd. →