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

Renovo, Inc. has 6 FDA 510(k) cleared medical devices. Based in Bend, US.

Historical record: 6 cleared submissions from 2017 to 2018. Primary specialty: General & Plastic Surgery.

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

6 devices

1–6 of 6

Reprocessed DePuy Mitek Ablation Wand

K173740 · NUJ Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed · General & Plastic Surgery

Reprocessed ArthoCare Ablation Wand

K173741 · NUJ Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed · General & Plastic Surgery

Reprocessed ArthroCare ENT Coblator

K172647 · NUJ Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed · General & Plastic Surgery

Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar Sleeves

K172097 · NLM Laparoscope, General & Plastic Surgery, Reprocessed · Gastroenterology & Urology

Reprocessed Covidien Trocar

K172093 · NLM Laparoscope, General & Plastic Surgery, Reprocessed · Gastroenterology & Urology

Reprocessed Shavers/Burs

K172092 · HRX Arthroscope · Orthopedic