# Ophthalmed, LLC

- Location (FDA's records): Alpharetta, GA
- FDA decisions: 3 (2002–2015): 3 510(k) clearances
- Product codes: HQF (2), GEX (1)
- Predicates its devices cite: 8 (3 its own); citations of its devices by later devices: 7 (3 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
- Synergetics, Inc.: 1 (https://510kreport.com/company/synergetics)
- Katalyst Surgical, LLC: 1 (https://510kreport.com/company/katalyst-surgical)
- Lightmed Corp.: 1 (https://510kreport.com/company/lightmed)
- Microvision, Inc.: 1 (https://510kreport.com/company/microvision)
- Surgical Technologies, Inc.: 1 (https://510kreport.com/company/surgical-technologies)

## Firms that cite its devices most
- Katalyst Surgical, LLC: 2 (https://510kreport.com/company/katalyst-surgical)
- Nidek, Inc.: 1 (https://510kreport.com/company/nidek)
- Vortex Surgical, Inc.: 1 (https://510kreport.com/company/vortex-surgical)

## Its most-cited devices
- K021696: 20G Sma Laser Fiber, Model LF20; 25G Sma Laser Fiber, Model LF25 (2002), cited by 4
- K050807: 20G Sma Laser Fiber, Model LF100 (2005), cited by 2
- K142830: Ophthalmed Bending Laser Probes (2015), cited by 1

## Recent decisions
- K142830: Ophthalmed Bending Laser Probes (Jun 25, 2015)
- K050807: 20G Sma Laser Fiber, Model LF100 (Sep 21, 2005)
- K021696: 20G Sma Laser Fiber, Model LF20; 25G Sma Laser Fiber, Model LF25 (Aug 20, 2002)

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