# Dornier

- Location (FDA's records): Kennesaw, GA
- FDA decisions: 3 (1999–2001): 3 510(k) clearances
- Product codes: LNS (2), GEX (1)
- Predicates its devices cite: 8 (0 its own); citations of its devices by later devices: 4 (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
- Dornier Medtech America, Inc.: 3 (https://510kreport.com/company/dornier-medtech-america)
- Dornier Surgical Products, Inc.: 2 (https://510kreport.com/company/dornier-surgical-products)
- Classy Lady by Mehl of Puerto Rico, Inc.: 1 (https://510kreport.com/company/classy-lady-by-mehl-of-puerto-rico)
- Sharplan Lasers, Inc.: 1 (https://510kreport.com/company/sharplan-lasers)
- Siemens Corp.: 1 (https://510kreport.com/company/siemens)

## Firms that cite its devices most
- Dornier Medtech America, Inc.: 2 (https://510kreport.com/company/dornier-medtech-america)
- Direx Systems Corp.: 1 (https://510kreport.com/company/direx-systems)
- Technomed Medical Systems, SA: 1 (https://510kreport.com/company/technomed-medical-systems)

## Its most-cited devices
- K011873: Dornier Lithotripter S (Doli S) & Dornier Lithotripter S-XP (Doli S-XP) (2001), cited by 3
- K011773: Dornier Lithotripter 140(Doli 140) (2001), cited by 1

## Recent decisions
- K011873: Dornier Lithotripter S (Doli S) & Dornier Lithotripter S-XP (Doli S-XP) (Aug 31, 2001)
- K011773: Dornier Lithotripter 140(Doli 140) (Jun 22, 2001)
- K984349: Dornier Medilas R (Feb 4, 1999)

Source page: https://510kreport.com/company/dornier