# Lite-Med, Inc.

- Location (FDA's records): Taipei, TW
- FDA decisions: 3 (2011–2023): 3 510(k) clearances
- Product codes: LNS (3)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 4 (1 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.: 2 (https://510kreport.com/company/dornier-medtech-america)
- Siemens Medical Solutions USA, Inc.: 2 (https://510kreport.com/company/siemens-medical-solutions-usa)
- KARL STORZ Endoscopy-America, Inc.: 1 (https://510kreport.com/company/karl-storz-endoscopy-america)
- Medispec, Ltd.: 1 (https://510kreport.com/company/medispec)

## Firms that cite its devices most
- Shenzhen Wikkon Precision Technologies Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-wikkon-precision-technologies)
- Comed Medical Systems Co., Ltd.: 1 (https://510kreport.com/company/comed-medical-systems)
- KARL STORZ Endoscopy-America, Inc.: 1 (https://510kreport.com/company/karl-storz-endoscopy-america)

## Its most-cited devices
- K103217: Lite-Med LM-9200 Elma (2011), cited by 3
- K142561: LM-9300 ELMA Lithotripter (2015), cited by 1

## Recent decisions
- K213772: LM-9300 Plus Lithotripter (Jan 19, 2023)
- K142561: LM-9300 ELMA Lithotripter (Mar 20, 2015)
- K103217: Lite-Med LM-9200 Elma (Sep 28, 2011)

Source page: https://510kreport.com/company/lite-med