FDA.reportPublic FDA data

CADENCE DEVICE, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30106591313010659131CADENCE DEVICE, INC.1N2026-01-01250 W KENSINGER DR STE 400 Cranberry Township PA US 16066

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1662151415286680K163654VersaOne fascial closure system bladed trocar, VersaOne fascial closure system bladeless trocar, VersaOne fascial closure system optical trocarGCJ2017-03-08
1662151360181313
1662151044072884
1662151092847845
1662151115539395
1662151144599394
1662151284971071
1662151323109700
1662151574919402
1662151588149276
1662151611228955
1662151773967640
1662151780098775
1662151939855283
1662151975756722

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GCJ12017-03-08