Medical Device Manufacturer · US , Bend , OR

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

6 submissions · 6 cleared · Since 2017

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - Renovo, Inc. General & Plastic Surgery ✕

3 devices

1-3 of 3

Cleared Mar 19, 2018

Reprocessed DePuy Mitek Ablation Wand

General & Plastic Surgery · 102d

Cleared Mar 05, 2018

Reprocessed ArthoCare Ablation Wand

General & Plastic Surgery · 88d

Cleared Feb 21, 2018

Reprocessed ArthroCare ENT Coblator

General & Plastic Surgery · 173d