FDA.reportPublic FDA data

VERIFY DIAGNOSTICS

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
00VERIFY DIAGNOSTICS5N2020-04-25D-122 Commerce Park Dr Barrie Ontario CA L4N 8W8

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
00870266000508VeriCheck Drug Test Cup - AMP500 COC150 MET500 MDMA500 OPI2000 PCP25 THC50 CR SG PH NI OX GL+1 705-812-4957support@verifydiagnostics.com
00870266000515VeriCheck Drug Test Cup - AMP500 COC150 MET500 MDMA500 OPI2000 OXY100 PCP25 THC50+1 705-812-4957support@verifydiagnostics.com
00870266000584VeriCheck Drug Test Cup - AMP1000 BAR300 BZO300 COC300 MET1000 MTD300 OPI2000 OXY100 PCP25 THC50+1 705-812-4957support@verifydiagnostics.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2501521290285430K103574PREGNANCY ONE STEP RAPID TESTLCX2011-07-28
2501521252709643
2501521688383470

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
LCX12011-07-28

GUDID#