Bethesda Medical Devices

FDA Regulatory Profile

Bethesda Medical Devices 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 July 16, 2026.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K261309Palisades™ Buttress Plate SystemJuly 16, 2026
K252113PRADO™ Lumbar Interbody Fusion SystemAugust 5, 2025