# Dio-Med Corp.

- Location (FDA's records): Cambridge Cb4 4ws England, GB
- FDA decisions: 7 (1981–1994): 7 510(k) clearances
- Product codes: GEX (6), DRS (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (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
- Slt-J, Ltd.: 2 (https://510kreport.com/company/slt-j)

## Its most-cited devices
- K914520: Diomed 25 Surgical Diode Laser, Urology Applicat (1993), cited by 1
- K914521: Diomed 25 Surgical Diode Laser, Gen Surg Applicat (1993), cited by 1

## Recent decisions
- K933525: Diomed 25 25W Surgical Diode Laser (Mar 1, 1994)
- K931776: Diomed 25 25W Surgical Diode Laser (Oct 19, 1993)
- K931212: Diomed 25 25W Surgical Diode Laser (Sep 23, 1993)
- K914519: Diomed 25 Surgical Diode Laser, Gynecology Applic (Sep 16, 1993)
- K914520: Diomed 25 Surgical Diode Laser, Urology Applicat (Jan 22, 1993)
- K914521: Diomed 25 Surgical Diode Laser, Gen Surg Applicat (Jan 15, 1993)
- K813267: Disposable Diaphragm Domes (Dec 14, 1981)

Source page: https://510kreport.com/company/dio-med