# APK Technology Co., Ltd.

- Location (FDA's records): Shenzhen, CN
- FDA decisions: 7 (1991–2025): 7 510(k) clearances
- Names in FDA's records: APK Technology Co., Ltd. (5); Apk Technology (2)
- Product codes: DQA (2), LRP (2), DXQ (1), FTC (1), DSA (1)
- 510(k) review time since 2016: median 60 days, against 140 for FDA's reviews in the same codes and years (3 of 3 faster)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 5 (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
- Shenzhen Caremed Medical Technology Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-caremed-medical-technology)
- Tytan Medical Corp.: 1 (https://510kreport.com/company/tytan-medical)
- Shenzhen Med-Link Electronics Tech Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-med-link-electronics-tech)
- Epic Medical Equipment Services, Inc.: 1 (https://510kreport.com/company/epic-medical-equipment-services)

## Firms that cite its devices most
- Edan Instruments, Inc.: 2 (https://510kreport.com/company/edan-instruments)
- Energetic Designs, Inc.: 1 (https://510kreport.com/company/energetic-designs)
- Andon Health Co, Ltd.: 1 (https://510kreport.com/company/andon-health)
- Authentic Medical: 1 (https://510kreport.com/company/authentic-medical)

## Its most-cited devices
- K102825: Blood Pressure Cuff (2011), cited by 3
- K170536: ECG Disposable Lead Wire (2017), cited by 2

## Recent decisions
- K250425: Ultraviolet Phototherapy Device (Apr 7, 2025)
- K172981: Reusable SpO2 Sensors, Disposable SpO2 Sensors (Jun 8, 2018)
- K170536: ECG Disposable Lead Wire (Apr 24, 2017)
- K102825: Blood Pressure Cuff (Mar 2, 2011)
- K082846: Apk SPO2 Pulse Oximeter Sensor (Apr 3, 2009)
- K903963: Kits and Trays for One Time Use Only (Jul 29, 1991)
- K903962: Instruments for One Time Use/ Disposable (Jul 29, 1991)

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