DeviceClearance

Product code MQG— Obstetrics/Gynecology

Geri Embryo Incubator and Geri Dish

Classification name
Accessory, Assisted Reproduction
Device class
Class 2
Regulation
21 CFR 884.6120
Advisory panel
Obstetrics/Gynecology
Total cleared
47
First cleared
Most recent

Market context for product code MQG

FDA has cleared 47 devices under product code MQG between 1998 and 2026, filed by 30 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code MQG

Recent clearances under product code MQG

Data sourced from openFDA. This site is unofficial and independent of the FDA.