Medical Device Manufacturer · US , Flemington , NJ

Geister Medizin Technik GmbH - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1994

Total

Cleared

Denied

Geister Medizin Technik GmbH has 6 FDA 510(k) cleared medical devices. Based in Flemington, US.

Latest FDA clearance: Jun 2025. Active since 1994. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Geister Medizin Technik GmbH Filter by specialty or product code using the sidebar.

Geister Medizin Technik GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Geister Medizin Technik GmbH

6 devices

1-6 of 6