# Teleflex Medical Sdn. Bhd.

- Location (FDA's records): Kamunting, MY
- FDA decisions: 3 (2026–2026): 3 510(k) clearances
- Product codes: EZL (2), CAH (1)
- Predicates its devices cite: 4 (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
- Teleflexmedical, Inc.: 2 (https://510kreport.com/company/teleflexmedical)
- Gibeck, Inc.: 2 (https://510kreport.com/company/gibeck)

## Recent decisions
- K262056: Rusch Latex Gold Foley Catheter (Aug 5, 2026)
- K252643: Iso-Gard Filter Straight; Humid-Vent Filter Compact Angled (May 15, 2026)
- K252537: Rusch SoftSimplastic Foley Catheters (Jan 20, 2026)

Source page: https://510kreport.com/company/teleflex-medical-sdn-bhd