Euroteknika

FDA Regulatory Profile

Euroteknika appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 4, 2025.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K232383iPhysio® SystemMarch 4, 2025
K083670UNIVERSAL, AESTHETICA, NATEA, NATURAJuly 23, 2009
K083669OBIJune 8, 2009