Teleflex Medical Sdn. Bhd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K252643 | Iso-Gard Filter Straight; Humid-Vent Filter Compact Angled | May 15, 2026 |
| K252537 | Rusch SoftSimplastic Foley Catheters | January 20, 2026 |