# Kingston Technologies, Inc.

- Location (FDA's records): Dayton, NJ
- FDA decisions: 6 (1988–1994): 6 510(k) clearances
- Product codes: KMF (2), MGP (1), FAD (1), MGQ (1), DQX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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
- Microvena Corp.: 1 (https://510kreport.com/company/microvena)

## Its most-cited devices
- K935232: Hydrotorque Guide Wire (1994), cited by 1

## Recent decisions
- K935232: Hydrotorque Guide Wire (Jul 20, 1994)
- K940814: Hydro-M (TM) Wound Gel (May 12, 1994)
- K940738: Kti HY-Q (TM) Wound Dressing (May 6, 1994)
- K925660: Kti Transparent Wound Dressing (Apr 20, 1993)
- K921502: Hysorb Wound Dressing (Sep 29, 1992)
- K882157: Panamex (TM) Ureteral Stent (Aug 2, 1988)

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