Aveo Fia-Aveo-1
Aveo Fia-Aveo-1 is a Class II device made by Conmed Corporation, cleared under FDA 510(k) K221945 on 28 Jul 2022 and listed in FDA GUDID since 12 Oct 2022 (UDI-DI 20653405987205), 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 | Number20653405987205 | Date12 Oct 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK221945 | Date28 Jul 2022 | StatusActive |
Official records
- AccessGUDID record 20653405987205
- FDA 510(k) database K221945
Across registries
- FDA 510(k) K221945 decided 28 Jul 2022 Active
- FDA GUDID UDI-DI 20653405987205 listed 12 Oct 2022 Listed
Timeline
- Cleared FDA 510(k) K221945
- Listed FDA GUDID 20653405987205
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Aveo
- Generic name
- Inert gas-enhanced endoscopic electrosurgical electrode, single-use
- Model / Ref / Catalog
- FIA-AVEO-1
- Primary DI / UDI-DI
- 20653405987205
- 510(k) Number
- FDA product code
- GEI
- GMDN term
- Inert gas-enhanced endoscopic electrosurgical electrode, single-use
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Ethylene Oxide
Similar devices in this category
Other devices filed under Inert gas-enhanced endoscopic electrosurgical electrode, single-use.