# Oasis Medikal Urunler Kimya Sanayi VE Tic A.S.

- Location (FDA's records): Durham, NC
- FDA decisions: 1 (2007–2007): 1 510(k) clearance
- Product codes: EZD (1)
- Predicates its devices cite: 7 (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
- Astra Tech, Inc.: 3 (https://510kreport.com/company/astra-tech)
- Coloplast Corp.: 2 (https://510kreport.com/company/coloplast)
- Astra Meditec AB: 1 (https://510kreport.com/company/astra-meditec)
- Rusch Intl.: 1 (https://510kreport.com/company/rusch-intl)

## Firms that cite its devices most
- Chengdu Daxan Innovative Medical Tech. Co., Ltd.: 1 (https://510kreport.com/company/chengdu-daxan-innovative-medical-tech)
- Well Lead Medical Co., Ltd.: 1 (https://510kreport.com/company/well-lead-medical)
- Dentsply Sirona: 1 (https://510kreport.com/company/dentsply-sirona)

## Its most-cited devices
- K062444: HI-Slip and HI-Slip Plus Single Use Hydrophilic Urinary Catheters and Kit (2007), cited by 3

## Recent decisions
- K062444: HI-Slip and HI-Slip Plus Single Use Hydrophilic Urinary Catheters and Kit (Feb 22, 2007)

Source page: https://510kreport.com/company/oasis-medikal-urunler-kimya-sanayi-ve-tic