Sfm Medical Devices GmbH

FDA Regulatory Profile

Sfm Medical Devices GmbH appears in FDA public data with 0 recalls, 3 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 6, 2024.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K241976nextaro® va, 15mm, 5µmSeptember 6, 2024
K240748nextaro® v, 20/20April 16, 2024
K183187nextaro Transfer System, nextaro vaMarch 15, 2019