# Quanta Dialysis Technologies, Ltd.

- Location (FDA's records): Alcester, GB
- FDA decisions: 4 (2020–2024): 4 510(k) clearances
- Product codes: KDI (3), ONW (1)
- Predicates its devices cite: 5 (3 its own); citations of its devices by later devices: 3 (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
- Home Dialysis Plus: 2 (https://510kreport.com/company/home-dialysis-plus)

## Its most-cited devices
- K210661: SC+ Hemodialysis Machine, SC+ Dialysate Cartridge, SC+ Blood Tubeset (2021), cited by 2
- K193670: SC+ Haemodialysis Machine, SC+ Dialysate Cartridge, SC+ Blood Tube Set (2020), cited by 1

## Recent decisions
- K242269: SC+ Hemodialysis Device (SC-14269); Dialysate Cartridge (SC-14656); Blood Tube Set (SC-14651) (Nov 1, 2024)
- K222067: SC+ Hemodialysis Device, SC+ Dialysate Cartridge, SC+ Blood Tube Set (Nov 10, 2022)
- K210661: SC+ Hemodialysis Machine, SC+ Dialysate Cartridge, SC+ Blood Tubeset (Aug 12, 2021)
- K193670: SC+ Haemodialysis Machine, SC+ Dialysate Cartridge, SC+ Blood Tube Set (Dec 23, 2020)

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