FondCircle FBP-W1
FondCircle FBP-W1 is a Class II device made by FondCircle Inc., listed in FDA GUDID since 14 Jan 2025 (UDI-DI 00850070979115), registry data as of 22 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 | Number00850070979115 | Date14 Jan 2025 | StatusListed |
Official records
- AccessGUDID record 00850070979115
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- FondCircle
- Generic name
- Automatic-inflation electronic sphygmomanometer, portable, arm/wrist
- Model / reference
- FBP-W1
- Primary DI / UDI-DI
- 00850070979115
- FDA product code
- DXN
- GMDN term
- Automatic-inflation electronic sphygmomanometer, portable, arm/wrist
- Device class
- Class II
- Regulation number
- 870.1130
- GUDID distribution status
- In Commercial Distribution
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