# Erbe Electromedizin GmbH

- Location (FDA's records): Dacula, GA
- FDA decisions: 2 (1990–1995): 2 510(k) clearances
- Product codes: GEI (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (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 that cite its devices most
- Aesculap, Inc.: 1 (https://510kreport.com/company/aesculap)
- Erbe USA, Inc.: 1 (https://510kreport.com/company/erbe-usa)

## Its most-cited devices
- K953738: Erbotom Icc 300 (1995), cited by 2

## Recent decisions
- K953738: Erbotom Icc 300 (Oct 16, 1995)
- K896055: Erbotom Acc 450 (Feb 13, 1990)

Source page: https://510kreport.com/company/erbe-electromedizin