Therasigma, LLC

FDA Regulatory Profile

Therasigma, LLC appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 26, 2021.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K202725ETD4000March 26, 2021
K201958ETD Family of Electrotherapy DevicesAugust 4, 2020