# Fiegert-Endotech Medizintechnik GmbH

- Location (FDA's records): Tuttlingen, DE
- FDA decisions: 1 (1998–1998): 1 510(k) clearance
- Product codes: FDS (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
- K974493: Fiegert Endotech Flexible Fiberoptic Endoscopes, Fiegert Endotech Flexible Video-Endoscopes (Mar 31, 1998)

Source page: https://510kreport.com/company/fiegert-endotech-medizintechnik