# Shenzhen Yicai Health Technology Co., Ltd.

- Location (FDA's records): Shenzhen, CN
- FDA decisions: 3 (2024–2025): 3 510(k) clearances
- Product codes: NUH (2), IRP (1)
- 510(k) review time since 2016: median 112 days, against 119 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 0 (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
- Hivox Biotek, Inc.: 2 (https://510kreport.com/company/hivox-biotek)
- Hong Qiangxing (Shenzhen) Electronics Limited: 1 (https://510kreport.com/company/hong-qiangxing-shenzhen-electronics)
- Jkh USA, LLC: 1 (https://510kreport.com/company/jkh-usa)

## Recent decisions
- K251623: Air Compression Therapy Device (K1002/K1006/K1007/K1008/K1061) (Sep 17, 2025)
- K250784: Transcutaneous Electrical Nerve Stimulator ( K6133/ K6134/ K6135/ K6136/ K6137/ K6138/ K6139/ K6140/ K6141/ K6142/ K6143/ K6144/ K6122) (Aug 21, 2025)
- K241119: Transcutaneous Electrical Nerve Stimulator (K6106) (Jul 22, 2024)

Source page: https://510kreport.com/company/shenzhen-yicai-health-technology