Renovo, Inc.
Renovo, Inc. holds FDA 510(k) medical device clearances, first cleared 2017, most recent 2018, with 1 FDA device recall on record.
Top product codes for Renovo, Inc.
FDA recalls by Renovo, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Renovo, Inc.
- K173740 — Reprocessed DePuy Mitek Ablation Wand
- K173741 — Reprocessed ArthoCare Ablation Wand
- K172647 — Reprocessed ArthroCare ENT Coblator
- K172097 — Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar Sleeves
- K172093 — Reprocessed Covidien Trocar
- K172092 — Reprocessed Shavers/Burs
Data sourced from openFDA. This site is unofficial and independent of the FDA.