# Diamedix Corp.

- Location (FDA's records): Miami, FL
- FDA decisions: 68 (1986–2011): 68 510(k) clearances
- Product codes: LLL (10), LFX (5), LSR (4), LGD (4), LRM (3), DHR (3), MID (3), DHN (2), CZW (2), KHW (2), LJM (2), LFY (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 8 (0 its own)
- Recalls linked to its devices: 9 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- DiaSorin, Inc.: 6 (https://510kreport.com/company/diasorin)
- Roche Diagnostics Corp.: 2 (https://510kreport.com/company/roche-diagnostics)

## Its most-cited devices
- K001767: Diamedix IS-CMV Igm Capture Test System (2000), cited by 2
- K981498: IS-Toxoplasma Igg Test System (1998), cited by 2
- K981867: IS-Vzu Igg Test System (1998), cited by 1
- K973177: Mago Automated Eia Processor (1997), cited by 1
- K001707: Diamedix IS-Toxoplasma Igm Capture Test System (2000), cited by 1
- K981163: Diamedix IS-CMV Igg Test System (1998), cited by 1

## Recent decisions
- K093101: MAGO 4S (Jan 21, 2011)
- K021394: Diamedix IS-Rheumatoid Factor Test System (Jul 9, 2002)
- K013956: Diamedix IS-Anti-B2 Glycoprotein I Screen (Jan 8, 2002)
- K013628: Diamedix IS-Anti-B2 Glycoprotein I Igg/Igm Test System (Dec 21, 2001)
- K012450: Diamedix IS-Anti-Cardiolipin Iga Test System (Oct 26, 2001)
- K012449: Diamedix IS-Anti-Cardiolipin Igg/Igm Test System (Oct 26, 2001)
- K012797: Diamedix IS-Anti-Gliadin Iga Test System (Sep 28, 2001)
- K012795: Diamedix IS-Anti-Gliadin Igg Test System (Sep 28, 2001)

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