# Shenzhen Jiantuo Electronics Co., Ltd.

- Location (FDA's records): Shenzhen, CN
- FDA decisions: 3 (2025–2025): 3 510(k) clearances
- Product codes: NUH (3)
- 510(k) review time since 2016: median 93 days, against 119 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 0 (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

## Recent decisions
- K253305: TENS AND EMS (TENS and Muscle Stimulator) (JT1065, JT1080, JT2080, JT9034) (Dec 31, 2025)
- K250360: TENS AND EMS (TENS and Muscle Stimulator) (JT8012C,JT8016,JT9020E,JT9026) (May 11, 2025)
- K250053: TENS AND EMS (TENS and Muscle Stimulator) (JT8012, JT8012B) (May 9, 2025)

Source page: https://510kreport.com/company/shenzhen-jiantuo-electronics