# Aesculap-Meditec GmbH

- Location (FDA's records): Irvine, CA
- FDA decisions: 3 (1997–1999): 3 510(k) clearances
- Product codes: GEX (3)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 7 (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
- Schwartz Electro-Optics, Inc.: 1 (https://510kreport.com/company/schwartz-electro-optics)
- Continuum Biomedical, Inc.: 1 (https://510kreport.com/company/continuum-biomedical)

## Firms that cite its devices most
- Wavelight Laser Technologie AG: 2 (https://510kreport.com/company/wavelight-laser-technologie)
- Sharplan Lasers, Inc.: 1 (https://510kreport.com/company/sharplan-lasers)
- Endo Technic Corp.: 1 (https://510kreport.com/company/endo-technic)
- Lumenis, Inc.: 1 (https://510kreport.com/company/lumenis)
- Phantom Technologies, Inc.: 1 (https://510kreport.com/company/phantom-technologies)
- Biolase Technology, Inc.: 1 (https://510kreport.com/company/biolase-technology)

## Its most-cited devices
- K964128: MCL 29 Dermablate Erbium Laser System (1997), cited by 6
- K983215: Multipulse CO2 Laser (1998), cited by 1

## Recent decisions
- K991993: Phacolase ER: Yag Laser (Nov 17, 1999)
- K983215: Multipulse CO2 Laser (Dec 4, 1998)
- K964128: MCL 29 Dermablate Erbium Laser System (Mar 17, 1997)

Source page: https://510kreport.com/company/aesculap-meditec