Geister Medizin Technik GmbH
Geister Medizin Technik GmbH holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2025.
Top product codes for Geister Medizin Technik GmbH
Recent clearances by Geister Medizin Technik GmbH
- K242759 — Geister K-Rex rongeurs
- K180610 — Geister retractor for neuro - and spine surgery
- K022823 — VALVULOTOME, RETROGRADE : 03-7500- 03-7510, ANTEGRADE 03-7520
- K030788 — KAMAR ANNULUS DILATOR + SIZER; GARRETT, COOLEY, AND DEBAKEY VESSEL DILATORS
- K982365 — ATRAUMATIC VASCULAR CLAMPS, MODEL #'S 22-XXXX, 23-XXXX, 03-60XX, 25-XXXX MICRO VASCULAR CLAMPS MODEL # 75-0XXX, ATRAUMAT
- K933699 — GEISTER SURGICAL INT'L BIPOLAR ENDOSCOPIC SURGICAL INSTRUMENTS
Data sourced from openFDA. This site is unofficial and independent of the FDA.