FDA.reportPublic FDA data

VIVORTE, INC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30106428153010642815VIVORTE, INC1N2020-04-251044 E Chestnut St Louisville KY US 40204

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
00868201000164Fortera - Calcium compound bone void filler (3 cc)5027147234info@vivorte.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1736462004962373K131133VIVORTE BVF LITEMQV2013-08-12
1736461930561591K130703VIVORTE BVFMBP2013-09-12

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MBP12013-09-12
MQV12013-08-12

PMN#

GUDID#