# Sunder Biomedical Tech. Co., Ltd.

- Location (FDA's records): Taichung City, TW
- FDA decisions: 3 (2001–2003): 3 510(k) clearances
- Product codes: FOZ (1), FIE (1), FJK (1)
- Predicates its devices cite: 1 (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 whose devices it cites most
- Arrow Intl., Inc.: 1 (https://510kreport.com/company/arrow-intl)

## Firms that cite its devices most
- Foshan Nanhai Bai HE Medical Technology Co., Ltd.: 1 (https://510kreport.com/company/foshan-nanhai-bai-he-medical-technology)

## Its most-cited devices
- K024007: Sunder Central Venous Catheter Kit, Models SD-3L55F30J and SD-3L70F30J (2003), cited by 1

## Recent decisions
- K024007: Sunder Central Venous Catheter Kit, Models SD-3L55F30J and SD-3L70F30J (Jul 14, 2003)
- K014140: Renax Hemodialysis Blood Tubing Set; Sunder Hemodialysis Blood Tubing Set (Nov 18, 2002)
- K003123: Renax a.V. Fistula Needle Sets (May 4, 2001)

Source page: https://510kreport.com/company/sunder-biomedical-tech