Maquet GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Maquet GmbH - FDA 510(k) Cleared Devices
Recent clearances: GSS610N21 Series Steam Sterilizer, Getinge GSS610N Series Steam Sterilizer, Getinge GSS67N Series Steam Sterilizer
3
Total
3
Cleared
0
Denied
Maquet GmbH, is a global medical device manufacturer with a manufacturing facility in Rastatt, Germany. The company specializes in General Hospital devices, serving healthcare facilities worldwide.
Maquet GmbH has received 3 FDA 510(k) clearances from 3 total submissions. All submissions focused on General Hospital devices. The company's regulatory activity spans from 2018 to 2022, with no recent submissions on record.
The company's cleared devices include steam sterilization systems designed for hospital use. These products represent core technologies in sterile reprocessing and infection control within general hospital settings.
This company profile reflects historical FDA 510(k) records. For detailed device names, product codes, and clearance dates, explore the full submission history.
510(k) submissions have been managed by Getinge as regulatory consultant.
FDA 510(k) Regulatory Record - Maquet GmbH
3 devices