# Dynamic Technology Corp.

- Location (FDA's records): Hsinchu, TW
- FDA decisions: 4 (1997–2002): 4 510(k) clearances
- Product codes: KDI (2), FJI (2)
- Predicates its devices cite: 8 (2 its own); citations of its devices by later devices: 2 (2 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
- Minntech Corp.: 2 (https://510kreport.com/company/minntech)
- National Medical Care, Medical Products Div., Inc.: 1 (https://510kreport.com/company/national-medical-care-medical-products-div)
- Gambro, Inc.: 1 (https://510kreport.com/company/gambro)
- Seratronics, Inc.: 1 (https://510kreport.com/company/seratronics)
- Cobe Laboratories, Inc.: 1 (https://510kreport.com/company/cobe-laboratories)

## Its most-cited devices
- K973291: Dynamic Hollow Fiber Dialyzer DC-Series (1997), cited by 2

## Recent decisions
- K011537: Dynamic Hollow Fiber Dialyzer DS-Series, Model: Polysulfone 100 HFS, Polysulfone 130 HFS (Jan 7, 2002)
- K990159: Dynamic Hollow Fiber Dialyzer DH-Series, Model AH 90111 (Apr 19, 1999)
- K982134: Dynamic Hollow Fiber Dialyzer DS-Series Model as-851 (Apr 14, 1999)
- K973291: Dynamic Hollow Fiber Dialyzer DC-Series (Dec 19, 1997)

Source page: https://510kreport.com/company/dynamic-technology