Reprocessed DePuy Mitek Ablation Wand
ReNovo, Inc.
RENOVO, INC.
FDA Registration(s)#
| Registration | FEI | Name | Status | Initial importer | Expiration year | Address |
|---|---|---|---|---|---|---|
| 3014023545 | 3014023545 | RENOVO, INC. | 1 | N | 2026-01-01 | 340 SW COLUMBIA ST Bend OR US 97702 |
Registered Device Listings#
| Registration key | Listing key | Premarket submission | Device | Product code | Decision date |
|---|---|---|---|---|---|
| 211427 | 2030138206 | K173741 | Reprocessed ArthoCare Ablation Wand | NUJ | 2018-03-05 |
| 211427 | 1143477685 | K173740 | Reprocessed DePuy Mitek Ablation Wand | NUJ | 2018-03-19 |
| 211427 | 1178649201 | K172647 | Reprocessed ArthroCare ENT Coblator | NUJ | 2018-02-21 |
| 211427 | 1352726919 | K172097 | Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar Sleeves | NLM | 2017-10-06 |
| 211427 | 1422744499 | K172093 | Reprocessed Covidien Trocar | NLM | 2017-10-05 |
| 211427 | 1579470534 | K172092 | Reprocessed Shavers/Burs | HRX | 2017-10-04 |
| 211427 | 1009610732 | ||||
| 211427 | 1041288751 | ||||
| 211427 | 1089112145 | ||||
| 211427 | 1174879093 | ||||
| 211427 | 1283042776 | ||||
| 211427 | 1286368290 | ||||
| 211427 | 1300566526 | ||||
| 211427 | 1310257243 | ||||
| 211427 | 1458366982 | ||||
| 211427 | 1512021555 | ||||
| 211427 | 1656377002 | ||||
| 211427 | 1940972182 | ||||
| 211427 | 1949911859 | ||||
| 211427 | 1990449278 | ||||
| 211427 | 2001390664 | ||||
| 211427 | 2019111218 | ||||
| 211427 | 2065748036 | ||||
| 211427 | 1025423461 | ||||
| 211427 | 1268274762 | ||||
| 211427 | 1430026738 | ||||
| 211427 | 1487573219 | ||||
| 211427 | 1751585133 | ||||
| 211427 | 2006493969 |
Product Codes Associated With Registrations#
PMN#
Reprocessed ArthoCare Ablation Wand
ReNovo, Inc.
Reprocessed ArthroCare ENT Coblator
ReNovo, Inc.
Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar Sleeves
Renovo, Inc.
Reprocessed Covidien Trocar
Renovo, Inc.
Reprocessed Shavers/Burs
Renovo, Inc.