MicroAire® 7020-ASP
by MicroAire Surgical Instruments LLC
MicroAire® 7020-ASP is a Class II device made by MicroAire Surgical Instruments LLC, cleared under FDA 510(k) K244026 on 25 Apr 2025 and listed in FDA GUDID since 1 Aug 2025 (UDI-DI 00847399017444), 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 | Number00847399017444 | Date1 Aug 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK244026 | Date25 Apr 2025 | StatusActive |
Official records
- AccessGUDID record 00847399017444
- FDA 510(k) database K244026
Across registries
- FDA 510(k) K244026 decided 25 Apr 2025 Active
- FDA GUDID UDI-DI 00847399017444 listed 1 Aug 2025 Listed
Timeline
- Cleared FDA 510(k) K244026
- Listed FDA GUDID 00847399017444
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- MicroAire®
- Generic name
- Liposuction system
- Model / reference
- 7020-ASP
- Primary DI / UDI-DI
- 00847399017444
- 510(k) Number
- FDA product code
- QPB
- GMDN term
- Liposuction system
- Device class
- Class II
- Regulation number
- 878.5040
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Liposuction system.