# Lightscalpel, LLC

- Location (FDA's records): Woodinville, WA
- FDA decisions: 6 (2012–2023): 6 510(k) clearances
- Names in FDA's records: Lightscalpel, LLC (5); Lightscalpel, Inc. (1)
- Product codes: GEX (6)
- Predicates its devices cite: 18 (6 its own); citations of its devices by later devices: 6 (6 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
- Lumenis, Inc.: 3 (https://510kreport.com/company/lumenis)
- Aesculight, LLC: 2 (https://510kreport.com/company/aesculight)
- Luxar Corp.: 2 (https://510kreport.com/company/luxar)
- Sharplan Lasers, Inc.: 2 (https://510kreport.com/company/sharplan-lasers)
- El.En Electronic Engineering Spa: 1 (https://510kreport.com/company/el-en-electronic-engineering)
- Alma Lasers, Inc.: 1 (https://510kreport.com/company/alma-lasers)
- Lutronic Corporation: 1 (https://510kreport.com/company/lutronic)

## Its most-cited devices
- K123037: Lightscalpel (2012), cited by 2
- K141658: Light Scalpel (2014), cited by 2
- K121471: Lightscalpel Family of Handpiece Tips for CO2 Surgical Lasers (2012), cited by 1
- K132661: Lightscalpel (2014), cited by 1

## Recent decisions
- K213669: Lightscalpel LS-4020 (Feb 15, 2023)
- K173827: LightScalpel (Sep 14, 2018)
- K141658: Light Scalpel (Oct 22, 2014)
- K132661: Lightscalpel (Jan 2, 2014)
- K123037: Lightscalpel (Nov 29, 2012)
- K121471: Lightscalpel Family of Handpiece Tips for CO2 Surgical Lasers (Jul 10, 2012)

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