FDA Device Establishments · JSON-LD · Markdown

RENOVO, INC.

FEI 3014023545 · Reprocess Single-Use Device · Status: Active

FEI Number3014023545
Owner / OperatorReNovo, Inc (#10054580)
Address340 SW COLUMBIA ST, Bend, OR, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)HWQ
Regulation § (21 CFR)888.4540
Proprietary namesReNovo, Inc.

External sources

Source: openFDA. Public-domain (CC0).