Beamer AVEO AVEO-ESU
Beamer AVEO-ESU is an inert gas-enhanced electrosurgical system (FDA Class II; FDA product code GEI, Electrosurgical, cutting & coagulation & accessories) made by Conmed Corporation, cleared under FDA 510(k) K214058 on 26 Aug 2022 and listed in FDA GUDID since 12 Oct 2022 (UDI-DI 20845854081508), 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 | Number20845854081508 | Date12 Oct 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK214058 | Date26 Aug 2022 | StatusActive |
Official records
- AccessGUDID record 20845854081508
- FDA 510(k) database K214058
Across registries
- FDA 510(k) K214058 decided 26 Aug 2022 Active
- FDA GUDID UDI-DI 20845854081508 listed 12 Oct 2022 Listed
Timeline
- Cleared FDA 510(k) K214058
- Listed FDA GUDID 20845854081508
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Beamer AVEO
- Generic name
- Inert gas-enhanced electrosurgical system
- Model / Ref / Catalog
- AVEO-ESU
- Primary DI / UDI-DI
- 20845854081508
- 510(k) Number
- FDA product code
- GEI
- GMDN term
- Inert gas-enhanced electrosurgical system
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
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