MQGClass II

Accessory, Assisted Reproduction

21 CFR 884.6120 / Obstetrics/Gynecology

MQG is the FDA product code for Accessory, Assisted Reproduction, a class II device type, regulated under 21 CFR 884.6120. As of 2026-09-10, FDA records hold 47 510(k) clearances under this code, the most recent dated 2026-08-19, and 9 recalls.

Classification record

Product code: MQG
Device name: Accessory, Assisted Reproduction
Regulation: 21 CFR 884.6120
Device class: Class II
Review panel: Obstetrics/Gynecology
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: Yes
Ingested clearances: 47
Ingested recalls: 9

Clearances, product code MQG

By decision year

47 clearances under product code MQG with a decision year between 1998 and 2026, 2000 the highest year at 9.

Show the numbers

510(k) clearances under FDA product code MQG by decision year
Year	Clearances
1998	1
1999	6
2000	9
2001	2
2002	4
2003	3
2004	1
2005	1
2006	1
2011	4
2012	1
2014	3
2016	2
2017	2
2018	3
2024	1
2025	1
2026	2

Applicants with the most clearances

Product code MQG

Applicants holding the most 510(k) clearances under product code MQG
Applicant	Clearances
Zander Medical Supplies, Inc.	5
Unisense Fertilitech A/S	4
<Genx> Intl., Inc.	3
GENEA BIOMEDX Pty Ltd.	3
At Medical UAB	2
Cook Ob/Gyn	2
Cook Incorporated	2
Kendro Laboratory Products, L.P.	2
PLANER Limited	2
Thermoquest Corp.	2

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 23 companies shown, in name order