# Tyece, Ltd.

- Location (FDA's records): Kowloon, HK
- FDA decisions: 4 (2015–2020): 4 510(k) clearances
- Names in FDA's records: Tyece , Ltd. (3); Tyece Limited (1)
- Product codes: NUH (2), NGX (2)
- 510(k) review time since 2016: median 117 days, against 147 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 3 (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 Dongdixin Technology Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-dongdixin-technology)
- Counter Scientific Development (Gz), Ltd.: 1 (https://510kreport.com/company/counter-scientific-development-gz)

## Firms that cite its devices most
- Shenzhen Kentro Medical Electronics Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-kentro-medical-electronics)
- Shenzhen Eapply Technology Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-eapply-technology)
- Hivox Biotek, Inc.: 1 (https://510kreport.com/company/hivox-biotek)

## Its most-cited devices
- K150386: Tyece OTC TENS Device (2015), cited by 3

## Recent decisions
- K200838: Tyece OTC TENS Model (Aug 12, 2020)
- K183454: Tyece OTC EMS System (Feb 26, 2019)
- K172241: Tyece OTC EMS System, Model EM35 (Nov 20, 2017)
- K150386: Tyece OTC TENS Device (Nov 5, 2015)

Source page: https://510kreport.com/company/tyece