# Renovo, Inc.

- Location (FDA's records): Bend, OR
- FDA decisions: 6 (2017–2018): 6 510(k) clearances
- Product codes: NUJ (3), NLM (2), HRX (1)
- 510(k) review time since 2016: median 95 days, against 88 for FDA's reviews in the same codes and years (1 of 4 faster)
- Predicates its devices cite: 22 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Arthrocare Corp.: 14 (https://510kreport.com/company/arthrocare)
- Depuy Mitek, A Johnson & Johnson Company: 3 (https://510kreport.com/company/depuy-mitek-a-johnson-johnson)
- Stryker Endoscopy: 1 (https://510kreport.com/company/stryker-endoscopy)
- Linvatec Corp.: 1 (https://510kreport.com/company/linvatec)
- Smith & Nephew, Inc.: 1 (https://510kreport.com/company/smith-nephew)
- Ethicon Endo-Surgery, Inc.: 1 (https://510kreport.com/company/ethicon-endo-surgery)
- United States Surgical, A Division of Tyco Healthc: 1 (https://510kreport.com/company/united-states-surgical-a-division-of-tyco-healthc)

## Recent decisions
- K173740: Reprocessed DePuy Mitek Ablation Wand (Mar 19, 2018)
- K173741: Reprocessed ArthoCare Ablation Wand (Mar 5, 2018)
- K172647: Reprocessed ArthroCare ENT Coblator (Feb 21, 2018)
- K172097: Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar Sleeves (Oct 6, 2017)
- K172093: Reprocessed Covidien Trocar (Oct 5, 2017)
- K172092: Reprocessed Shavers/Burs (Oct 4, 2017)

Source page: https://510kreport.com/company/renovo