Teleflex Medical Sdn. Bhd.

FDA Regulatory Profile

Teleflex Medical Sdn. Bhd. appears in FDA public data with 0 recalls, 2 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 15, 2026.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K252643Iso-Gard Filter Straight; Humid-Vent Filter Compact AngledMay 15, 2026
K252537Rusch SoftSimplastic Foley CathetersJanuary 20, 2026