# Komet Medical

- Location (FDA's records): Savannah, GA
- FDA decisions: 3 (1994–1999): 3 510(k) clearances
- Product codes: GFF (1), HBE (1), HBB (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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
- Von Zeppelin GmbH: 1 (https://510kreport.com/company/von-zeppelin)
- Aesculap, Inc.: 1 (https://510kreport.com/company/aesculap)
- Medicon EG: 1 (https://510kreport.com/company/medicon-eg)

## Its most-cited devices
- K991625: Komet XK-95 Perforator Motor (MI-102) (1999), cited by 2
- K984035: XK-95 High Speed Motor Drill System (1999), cited by 1

## Recent decisions
- K991625: Komet XK-95 Perforator Motor (MI-102) (Jul 30, 1999)
- K984035: XK-95 High Speed Motor Drill System (Jun 3, 1999)
- K943758: Surgical Bur (Aug 22, 1994)

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