# Seers Technology Co., Ltd.

- Location (FDA's records): Pittsburgh, PA
- FDA decisions: 2 (2012–2026): 2 510(k) clearances
- Product codes: DXN (1), MWJ (1)
- Predicates its devices cite: 2 (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
- A&D Engineering, Inc.: 1 (https://510kreport.com/company/a-d-engineering)
- Wellysis Corp.: 1 (https://510kreport.com/company/wellysis)

## Recent decisions
- K253384: mobiCARE Cardiac Monitoring System (mobiCARE-MC200M, mobiCARE-MC200ML, mobiCARE-MC200M7, mobiCARE-MC200ML7) (Jun 25, 2026)
- K120545: HX-461 (Oct 23, 2012)

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