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Myndtec, Inc.

FDA Regulatory Profile

Myndtec, Inc. 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 June 25, 2024.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K233006MyndMove, MyndMove 2.0June 25, 2024
K212149MyndMove 2.0March 3, 2022
K170564MyndMove System, MyndMove Functional Electrical StimulatorAugust 30, 2017

FDA data resources