Geister Medizin Technik GmbH - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
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.
FDA 510(k) cleared devices by Geister Medizin Technik GmbH
6 devices
Cleared
Jun 06, 2025
Geister K-Rex rongeurs
Neurology
267d
Cleared
Aug 29, 2018
Geister retractor for neuro - and spine surgery
General & Plastic Surgery
174d
Cleared
Jul 01, 2004
VALVULOTOME, RETROGRADE : 03-7500- 03-7510, ANTEGRADE 03-7520
Cardiovascular
675d
Cleared
Jul 12, 2003
KAMAR ANNULUS DILATOR + SIZER
Cardiovascular
122d
Cleared
Apr 08, 1999
ATRAUMATIC VASCULAR CLAMPS, MODEL #'S 22-XXXX, 23-XXXX, 03-60XX, 25-XXXX...
Cardiovascular
275d
Cleared
Jan 27, 1994
GEISTER SURGICAL INT'L BIPOLAR ENDOSCOPIC SURGICAL INSTRUMENTS
General & Plastic Surgery
182d