# Ergoline GmbH

- Location (FDA's records): Tuttlingen, Baden Wurttemberg, DE
- FDA decisions: 3 (2006–2022): 3 510(k) clearances
- Product codes: ISD (2), DRG (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 2 (1 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
- Scottcare Corporation: 1 (https://510kreport.com/company/scottcare)
- Lode Corp.: 1 (https://510kreport.com/company/lode)

## Firms that cite its devices most
- Scottcare Corporation: 1 (https://510kreport.com/company/scottcare)

## Its most-cited devices
- K212883: ers2 - ergoline Rehabilitation System (2022), cited by 1
- K053078: Ergoselect 100 K/P, Ergoselect 200 K/P (2006), cited by 1

## Recent decisions
- K212883: ers2 - ergoline Rehabilitation System (Jul 15, 2022)
- K112121: Ergoselect/GE (Oct 31, 2012)
- K053078: Ergoselect 100 K/P, Ergoselect 200 K/P (Apr 27, 2006)

Source page: https://510kreport.com/company/ergoline