# Geotek Medikal Ltd Sti

- Location (FDA's records): Ankara, TR
- FDA decisions: 2 (2017–2023): 2 510(k) clearances
- Product codes: KNW (1), ITX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K223300: Estacore-Pro Automatic Biopsy Needle, Geotek Semiautomatic Biopsy Needle, Maxicore-M Automatic Biopsy Gun Needle, Maxicore-M Automatic Biopsy Needle and Instrument (Apr 21, 2023)
- K170741: GTK Disposable Needle Guides (Jun 1, 2017)

Source page: https://510kreport.com/company/geotek-medikal-sti