# Kelsey, Inc.

- Location (FDA's records): Catonsville, MD
- FDA decisions: 1 (2007–2007): 1 510(k) clearance
- Product codes: GEX (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 1 (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
- Diomed, Inc.: 1 (https://510kreport.com/company/diomed)
- Indigo Medical, Inc.: 1 (https://510kreport.com/company/indigo-medical)
- Ethicon Endo-Surgery, Inc.: 1 (https://510kreport.com/company/ethicon-endo-surgery)
- Endocare, Inc.: 1 (https://510kreport.com/company/endocare)

## Firms that cite its devices most
- Novian Health, Inc.: 1 (https://510kreport.com/company/novian-health)

## Its most-cited devices
- K070353: Kelsey Intersitital Laser Therapy System (2007), cited by 1

## Recent decisions
- K070353: Kelsey Intersitital Laser Therapy System (May 2, 2007)

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