Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1178649201
Device Listing 1178649201
Listing Summary
#
Listing key
1178649201
Premarket submission
K172647
Device
Reprocessed ArthroCare ENT Coblator
Applicant
Renovo, Inc.
Product code
NUJ
Decision date
2018-02-21
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
211427
3014023545
3014023545
RENOVO, INC.
1
N
2026-01-01
340 SW COLUMBIA ST Bend OR US 97702