FDA.reportPublic FDA data

OUI LAB INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30124777153012477715OUI LAB INC.1Y2026-01-0115362 Valley Blvd City of Industry CA US 91746

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
00850013300006IntiMD 8.5 fl oz Water Based Bottle(626) 315-8531support@intimd.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2977651314661961K213116Everyway Incontinence Stimulation SystemKPI2021-12-03
2977651632329425K051295I-D GLIDENUC2006-02-15
2977651004301684
2977651162500113
2977651231745792
2977651496339915
2977651514449994
2977651521077179
2977651658326011
2977651703837467
2977651979688702

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
KPI12021-12-03
NUC12006-02-15

GUDID#