Company ยท US
Renovo, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2017 to 2018. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Mar 19, 2018 | K173740 | Reprocessed DePuy Mitek Ablation Wand Renovo, Inc. | NUJ |
| Mar 5, 2018 | K173741 | Reprocessed ArthoCare Ablation Wand Renovo, Inc. | NUJ |
| Feb 21, 2018 | K172647 | Reprocessed ArthroCare ENT Coblator Renovo, Inc. | NUJ |
| Oct 6, 2017 | K172097 | Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar Sleeves Renovo, Inc. | NLM |
| Oct 5, 2017 | K172093 | Reprocessed Covidien Trocar Renovo, Inc. | NLM |
| Oct 4, 2017 | K172092 | Reprocessed Shavers/Burs Renovo, Inc. | HRX |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 19, 2021 | ReNovo, Inc. Various reprocessed products:
PROVISION, Reprocessed Smith and Nephew Arthroscopic Shavers, STERILE EO;
PROVISION Reprocessed Depy Mitek Ablation Electrodes, VAPR COOLPULSE 90 deg;
PROVISION Reproce Open, Classified |
HRX | None listed |