Medical Device Manufacturer · US , Plainville , MA

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

33 submissions · 33 cleared · Since 1997

Recent clearances: MODIFICATION TO ENDIUS MINIT POSTERIOR CERVICAL AND UPPER THORACIC FIXATION SYSTEM, ENDIUS TITLE 2 POLY AXIAL SPINAL SYSTEM, ENDIUS MINIT POSTERIOR CERVICAL AND UPPER THORACIC FIXATION SYSTEM

33
Total
33
Cleared
0
Denied

Endius, Inc. has 33 FDA 510(k) cleared orthopedic devices. Based in Plainville, US.

Historical record: 33 cleared submissions from 1997 to 2008.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

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

33 devices
1-12 of 33
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