Vivace Pro, Vybe Rf II
Vivace Pro, Vybe Rf II is an electrosurgical system generator (FDA Class II; FDA product code GEI, Electrosurgical, Cutting & Coagulation & Accessories) made by shenb Co., Ltd., cleared under FDA 510(k) K241535 on 25 Sep 2024 and listed in FDA GUDID since 22 Apr 2026 (UDI-DI 08800017101002), 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 | Number08800017101002 | Date22 Apr 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK241535 | Date25 Sep 2024 | StatusActive |
Official records
- AccessGUDID record 08800017101002
- FDA 510(k) database K241535
Across registries
- FDA 510(k) K241535 decided 25 Sep 2024 Active
- FDA GUDID UDI-DI 08800017101002 listed 22 Apr 2026 Listed
Timeline
- Cleared FDA 510(k) K241535
- Listed FDA GUDID 08800017101002
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Generic name
- Electrosurgical system generator
- Model / reference
- VYBE RF II
- Primary DI / UDI-DI
- 08800017101002
- 510(k) Number
- FDA product code
- GEI
- GMDN term
- Electrosurgical system generator
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
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