Medical Device Manufacturer · US , Plymouth , MN

Sterilmed, Inc. - FDA 510(k) Cleared Devices

64 submissions · 64 cleared · Since 2001

Recent clearances: Reprocessed DECANAV™ Electrophysiology Catheter, Reprocessed ViewFlex™ Xtra ICE Catheter, Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue Technology

64
Total
64
Cleared
0
Denied

Sterilmed, Inc. has 64 FDA 510(k) cleared medical devices. Based in Plymouth, US.

Latest FDA clearance: Oct 2024. Active since 2001.

Browse the FDA 510(k) cleared devices submitted by Sterilmed, Inc. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Libra Medical and Libramedical, Inc..

FDA 510(k) Regulatory Record - Sterilmed, Inc.

64 devices
1-12 of 64

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