# Celon AG Medical Instruments

- Location (FDA's records): Teltow, DE
- FDA decisions: 2 (2003–2008): 2 510(k) clearances
- Product codes: GEI (2)
- Predicates its devices cite: 8 (0 its own); citations of its devices by later devices: 6 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Arthrocare Corp.: 3 (https://510kreport.com/company/arthrocare)
- Somnus Medical Technologies, Inc.: 2 (https://510kreport.com/company/somnus-medical-technologies)
- Erbe USA, Inc.: 2 (https://510kreport.com/company/erbe-usa)
- Keymed (Medical & Industrial Equipment), Ltd.: 1 (https://510kreport.com/company/keymed-medical-industrial-equipment)

## Firms that cite its devices most
- Olympus Winter & Ibe GmbH: 2 (https://510kreport.com/company/olympus-winter-ibe)
- Byrne Medical, Inc.: 1 (https://510kreport.com/company/byrne-medical)
- Sutter Medizintechnik GmbH: 1 (https://510kreport.com/company/sutter-medizintechnik)
- Keymed (Medical & Industrial Equipment), Ltd.: 1 (https://510kreport.com/company/keymed-medical-industrial-equipment)
- Genii, Inc.: 1 (https://510kreport.com/company/genii)

## Its most-cited devices
- K032838: Celon Ent System (2003), cited by 3
- K073207: Olympus Esg-100, Model WB991046; Olympus Afu-100, Model WB950167 (2008), cited by 3

## Recent decisions
- K073207: Olympus Esg-100, Model WB991046; Olympus Afu-100, Model WB950167 (May 8, 2008)
- K032838: Celon Ent System (Sep 26, 2003)

Source page: https://510kreport.com/company/celon-ag-medical-instruments