MGIClass III

Aspirator, Ultrasonic

Unknown

MGI is the FDA product code for Aspirator, Ultrasonic, a class III device type. As of 2026-09-10, FDA records hold one 510(k) clearance under this code, the most recent dated 1992-03-27, and no recalls.

Classification record

Product code: MGI
Device name: Aspirator, Ultrasonic
Device class: Class III
Review panel: Unknown
Submission type: Contact ODE
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 1
Ingested recalls: 0

Clearances, product code MGI

By decision year

1 clearance under product code MGI with a decision year between 1992 and 1992, 1992 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code MGI by decision year
Year	Clearances
1992	1

Applicants with the most clearances

Product code MGI

Applicants holding the most 510(k) clearances under product code MGI
Applicant	Clearances
Sharplan Lasers, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code MGI.

Recent clearances

Product code MGI

K913848Class IIISharplan Model Ultra Ultrasonic Surg AspiratorSharplan Lasers, Inc. / cleared 1992-03-27

Recent recalls

Product code MGI

FDA records show no recalls under product code MGI.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)