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MicroAire® 7020

by MicroAire Surgical Instruments LLC

MicroAire® 7020 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 00847399017413), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K244026

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00847399017413 UDI-DI Date1 Aug 2025ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK244026 Date25 Apr 2025DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K244026 decided 25 Apr 2025 Active
  • FDA GUDID UDI-DI 00847399017413 listed 1 Aug 2025 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K244026
  2. Listed FDA GUDID 00847399017413

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
MicroAire®
Generic name
Liposuction system
Model / reference
7020
Primary DI / UDI-DI
00847399017413
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

Related devices

Category: Liposuction system

Cleared under the same submission (K244026)

Similar devices in this category

Other devices filed under Liposuction system.

Other devices from MicroAire Surgical Instruments LLC

See all devices from MicroAire Surgical Instruments LLC →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)