# Geister Medizin Technik GmbH

- Location (FDA's records): Tuttlingen, DE
- FDA decisions: 6 (1994–2025): 6 510(k) clearances
- Product codes: HAE (1), GEI (1), GZT (1), DXC (1), MGZ (1), DWP (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Aesculap, Inc.: 2 (https://510kreport.com/company/aesculap)
- Fehling Instruments GmbH & Co. KG: 1 (https://510kreport.com/company/fehling-instruments)
- V. Mueller Neuro/Spine: 1 (https://510kreport.com/company/v-mueller-neuro-spine)
- KLS-Martin L.P.: 1 (https://510kreport.com/company/kls-martin)
- Codman & Shurtleff, Inc.: 1 (https://510kreport.com/company/codman-shurtleff)

## Firms that cite its devices most
- Fetzer Medical GmbH & Co. KG: 1 (https://510kreport.com/company/fetzer-medical)
- Instrumed International, Inc.: 1 (https://510kreport.com/company/instrumed-international)
- Integra LifeSciences Corporation: 1 (https://510kreport.com/company/integra-lifesciences)
- SurGenTec, LLC: 1 (https://510kreport.com/company/surgentec)

## Its most-cited devices
- K030788: Kamar Annulus Dilator + Sizer; Garrett, Cooley, and Debakey Vessel Dilators (2003), cited by 3
- K180610: Geister retractor for neuro - and spine surgery (2018), cited by 1

## Recent decisions
- K242759: Geister K-Rex rongeurs (Jun 6, 2025)
- K180610: Geister retractor for neuro - and spine surgery (Aug 29, 2018)
- K022823: Valvulotome, Retrograde : 03-7500- 03-7510, Antegrade 03-7520 (Jul 1, 2004)
- K030788: Kamar Annulus Dilator + Sizer; Garrett, Cooley, and Debakey Vessel Dilators (Jul 12, 2003)
- K982365: Atraumatic Vascular Clamps, Model #'S 22-XXXX, 23-XXXX, 03-60XX, 25-XXXX Micro Vascular Clamps Model # 75-0XXX, Atraumat (Apr 8, 1999)
- K933699: Geister Surgical Int'l Bipolar Endoscopic Surgical Instruments (Jan 27, 1994)

Source page: https://510kreport.com/company/geister-medizin-technik
