# Oticon A/S

- Location (FDA's records): Smorum, DK
- FDA decisions: 2 (1995–2014): 2 510(k) clearances
- Product codes: KLW (1), ESD (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 1 (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 whose devices it cites most
- Gn Resound A/S: 1 (https://510kreport.com/company/gn-resound-a-s)
- Phonak, Inc.: 1 (https://510kreport.com/company/phonak)

## Firms that cite its devices most
- Kw Ear Lab, Inc.: 1 (https://510kreport.com/company/kw-ear-lab)

## Its most-cited devices
- K133308: Tinnitus Soundsupport (2014), cited by 1

## Recent decisions
- K133308: Tinnitus Soundsupport (Mar 18, 2014)
- K951002: Amendments to Multifocus (Sep 18, 1995)

Source page: https://510kreport.com/company/oticon-a-s