# Sharplight Technologies, Ltd.

- Location (FDA's records): Zichron Yaacov, IL
- FDA decisions: 4 (2008–2023): 4 510(k) clearances
- Product codes: GEX (4)
- Predicates its devices cite: 9 (2 its own); citations of its devices by later devices: 8 (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
- Alma Lasers, Inc.: 2 (https://510kreport.com/company/alma-lasers)
- Cutera, Inc.: 2 (https://510kreport.com/company/cutera)
- Palomar Medical Technologies, Inc.: 1 (https://510kreport.com/company/palomar-medical-technologies)
- Pollogen, Ltd.: 1 (https://510kreport.com/company/pollogen)
- Medic Sharplight, Ltd.: 1 (https://510kreport.com/company/medic-sharplight)

## Firms that cite its devices most
- M&T S.R.L.: 2 (https://510kreport.com/company/m-t)
- Viora, Ltd.: 1 (https://510kreport.com/company/viora)
- Bios S.R.L.: 1 (https://510kreport.com/company/bios)
- Sciton, Inc: 1 (https://510kreport.com/company/sciton)
- Quanta System Spa: 1 (https://510kreport.com/company/quanta-system)

## Its most-cited devices
- K111303: Dermatological Treatment Device Family (2011), cited by 7
- K082876: Beamax/ Formax Pulsed Light Device Family (2008), cited by 1

## Recent decisions
- K233304: Omnimax S3, Omnimax S4 (Dec 22, 2023)
- K173169: Rapid Family (Nov 20, 2017)
- K111303: Dermatological Treatment Device Family (Dec 21, 2011)
- K082876: Beamax/ Formax Pulsed Light Device Family (Nov 10, 2008)

Source page: https://510kreport.com/company/sharplight-technologies