FDA.reportPublic FDA data

UROLOGIX, LLC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
21339363000718675UROLOGIX, LLC1N2026-01-0113355 10th Ave N. Suite 110 Plymouth MN US 55441

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
M87689290Prostiva Hand Piece - Prostiva RF Therapy Hand Piece888.475.0772customerservice@urologix.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1916882044902852P970008TARGIS (T3) SYSTEMMEQ1997-08-22
1916881821135161K113380PROSTIVA RF THERAPY HAND PIECE PROSTIVA RF THERAPY RF GENERATORGEI2012-11-15

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GEI12012-11-15
MEQ11997-08-22

PMA#

89 records. Showing 1-40. Next

PMN#

GUDID#