# Shenzhen Future Electronic Co., Ltd.

- Location (FDA's records): Shenzhen, CN
- FDA decisions: 3 (2022–2025): 3 510(k) clearances
- Product codes: IRP (2), NUH (1)
- 510(k) review time since 2016: median 153 days, against 103 for FDA's reviews in the same codes and years (0 of 3 faster)
- Predicates its devices cite: 4 (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
- Shenzhen Osto Technology Company Limited: 2 (https://510kreport.com/company/shenzhen-osto-technology)
- Shenzhen Ruiyi Business Technology Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-ruiyi-business-technology)
- Shenzhen Dongjilian Electronics Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-dongjilian-electronics)

## Firms that cite its devices most
- NormaTec Industries, LP: 1 (https://510kreport.com/company/normatec-industries)

## Its most-cited devices
- K213745: Air Compression Therapy Device, model: ST-502 (2022), cited by 1

## Recent decisions
- K251662: Air Compression Therapy Device (ST-504); Air Compression Therapy Device (ST-505); Air Compression Therapy Device (ST-506); Air Compression Therapy Device (ST-507) (Nov 13, 2025)
- K221092: Transcutaneous Electrical Nerve Stimulator Model: ST-304 (Sep 13, 2022)
- K213745: Air Compression Therapy Device, model: ST-502 (Mar 31, 2022)

Source page: https://510kreport.com/company/shenzhen-future-electronic