# Litecure, LLC

- Location (FDA's records): Newark, DE
- FDA decisions: 7 (2007–2018): 7 510(k) clearances
- Product codes: GEX (3), ILY (3), PDZ (1)
- Predicates its devices cite: 16 (2 its own); citations of its devices by later devices: 3 (2 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
- Biolitec, Inc.: 2 (https://510kreport.com/company/biolitec)
- Sciton, Inc: 2 (https://510kreport.com/company/sciton)
- Eltech S.R.L: 2 (https://510kreport.com/company/eltech)
- Intermedic Arfran, SA: 1 (https://510kreport.com/company/intermedic-arfran)
- Quanta System Spa: 1 (https://510kreport.com/company/quanta-system)
- Biotex, Inc.: 1 (https://510kreport.com/company/biotex)
- Laserscope: 1 (https://510kreport.com/company/laserscope)
- B&W Tek, Inc.: 1 (https://510kreport.com/company/b-w-tek)

## Firms that cite its devices most
- Eltech S.R.L: 1 (https://510kreport.com/company/eltech)

## Its most-cited devices
- K070400: LC Therapy, Model LCT-1000 (2007), cited by 2
- K123014: Litecure Therapy System Model LTS-1500 (2013), cited by 1

## Recent decisions
- K173067: LightForce LTS Model 1000, 1500, 2500, and 4000 (Feb 22, 2018)
- K123014: Litecure Therapy System Model LTS-1500 (Mar 29, 2013)
- K123031: BWF-5 Medical Laser Series (Dec 3, 2012)
- K121487: Litecure Therapy Compact (Jun 12, 2012)
- K103511: Litecure Therapy System (Jan 25, 2011)
- K093087: BWF-5 Medical Laser Series (May 12, 2010)
- K070400: LC Therapy, Model LCT-1000 (Feb 28, 2007)

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