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Regenesis Biomedical, Inc.

FDA Regulatory Profile

Regenesis Biomedical, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 4 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 24, 2023.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K223620Reprieve by RegenesisTMMay 24, 2023
K131979PROVANT THERAPY SYSTEMDecember 13, 2013
K091791PROVANT SYSTEM, MODEL 4201April 7, 2010
K972093REGENESIS MODEL 42October 21, 1997

FDA data resources