# Diomedics, Inc.

- Location (FDA's records): Gainesville, FL
- FDA decisions: 3 (1993–2008): 3 510(k) clearances
- Product codes: ILY (1), FTC (1), GEX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 7 (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 that cite its devices most
- Life Without Pain, LLC: 1 (https://510kreport.com/company/life-without-pain)
- Cottonwood Vessel Corporation: 1 (https://510kreport.com/company/cottonwood-vessel)
- Quantum Devices, Inc.: 1 (https://510kreport.com/company/quantum-devices)
- Alma Lasers, Inc.: 1 (https://510kreport.com/company/alma-lasers)
- Varaya Photoceuticals, LLC: 1 (https://510kreport.com/company/varaya-photoceuticals)
- Photo Therapeutics Limited: 1 (https://510kreport.com/company/photo-therapeutics)
- Spectrum Laser & Technologies: 1 (https://510kreport.com/company/spectrum-laser-technologies)

## Its most-cited devices
- K982546: Phaser-2000 (1998), cited by 7

## Recent decisions
- K073503: Versa Lite (Jan 23, 2008)
- K982546: Phaser-2000 (Sep 22, 1998)
- K926224: Diomedics Surgi Light/Light Touch Optical Fibers (Jul 22, 1993)

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