# Sfm Medical Devices GmbH

- Location (FDA's records): Waechtersbach, DE
- FDA decisions: 3 (2019–2024): 3 510(k) clearances
- Product codes: LHI (3)
- 510(k) review time since 2016: median 63 days, against 166 for FDA's reviews in the same codes and years (3 of 3 faster)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 2 (2 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
- Medimop Medical Projects, Ltd.: 1 (https://510kreport.com/company/medimop-medical-projects)

## Its most-cited devices
- K183187: nextaro Transfer System, nextaro va (2019), cited by 2

## Recent decisions
- K241976: nextaro® va, 15mm, 5µm (Sep 6, 2024)
- K240748: nextaro® v, 20/20 (Apr 16, 2024)
- K183187: nextaro Transfer System, nextaro va (Mar 15, 2019)

Source page: https://510kreport.com/company/sfm-medical-devices