BENVENUE MEDICAL, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30070336083007047261BENVENUE MEDICAL, INC.1N2020-04-254590 Patrick Henry Dr Santa Clara CA US 95054

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00813478020001Kiva - Kiva VCF Treatment System, Fisrt Fracture Kit, Right(800) 997-7463info@benvenuemedical.com
00813478020018Kiva - Kiva VCF Treatment System, Additional Fracture Kit, Right(800) 997-7463info@benvenuemedical.com
00813478020025Kiva - Kiva VCF Treatment System, First Fracture Kit, Left(800) 997-7463info@benvenuemedical.com
00813478020032Kiva - Kiva VCF Treatment System, Additional Fracture Kit, Left(800) 997-7463info@benvenuemedical.com
00813478020049Kiva - Kiva VCF Treatment System, First Fracture, Right(800) 997-7463info@benvenuemedical.com
00813478020056Kiva - Kiva VCF Treatment System, First Fracture, Left(800) 997-7463info@benvenuemedical.com
00813478020377Luna 3D - Luna 3D Accessory Kit(800) 997-7463info@benvenuemedical.com
00813478020391Luna 3D - Luna 3D Lordotic Accessory Kit(800) 997-7463info@benvenuemedical.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
670741779146535K183560Luna 3D GEN2 Interbody Fusion SystemMAX2019-05-23
670741040339148K162431Luna 3D Interbody Fusion SystemMAX2016-11-17
670741746150625K142023LUNA INTERBODY SYSTEMMAX2014-11-20
670741345844348
670742028785386

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MAX32019-05-23

PMN#

GUDID#

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