# Dimesol, Inc.

- Location (FDA's records): Lewisberry, PA
- FDA decisions: 2 (2018–2018): 2 510(k) clearances
- Product codes: FJK (1), FIE (1)
- Predicates its devices cite: 5 (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
- Nipro Medical Corporation: 2 (https://510kreport.com/company/nipro-medical)
- Jms North America Corp.: 1 (https://510kreport.com/company/jms-north-america)
- Jms Co., Ltd.: 1 (https://510kreport.com/company/jms)
- Exelint Intl. Co.: 1 (https://510kreport.com/company/exelint-intl)

## Recent decisions
- K171505: Dimesol Disposable AV Fistula Needle Set (Non-Safety Series) and Dimesol Disposable AV Fistula Needle Set (Safety Series) (May 17, 2018)
- K171952: Dimesol Tubing Sets for Hemodialysis (Mar 30, 2018)

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