Bio-Dyne, Inc.

FDA Regulatory Profile

Bio-Dyne, Inc. has 0 FDA recalls, 0 inspections, 3 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Mar 8, 1990

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances3Oct 4, 2026Not statedCurrent
Inspections0Oct 27, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K900691BIODYNE INSTRUMENT WIPESMar 8, 1990
K883984HEMORX COLD PACKDec 22, 1988
K864261MODEL 3500 INFANT RESPIRATION & HEART RATE MONITORMar 27, 1987