# RENOVO, INC.

FEI: 3014023545
Status: Active
Establishment types: Reprocess Single-Use Device
Owner/operator: ReNovo, Inc (#10054580)

Address: 340 SW COLUMBIA ST, Bend, OR, US



## Products

Total registered: 1
Top product codes: HWQ
Regulation §: 888.4540

Proprietary names: ReNovo, Inc.

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223014023545%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3014023545