FDA.reportPublic FDA data

NUMOTECH, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
20305951000518730NUMOTECH, INC.1N2026-01-019420 RESEDA BLVD., SUITE 504 Northridge CA US 91324

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
00860010630600Numobag Kit - Extremity-oxygenation hyperbaric chamber, non-powered877-686-6832numotech@earthlink.net

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
758441126140465K981949NUMOBAGKPJ1999-02-03
758441599129888K943433TOTAL CONTACT SEAT RIPPLE SYSTEMIOQ1995-07-31
758441867875754
758442013133360

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
KPJ11999-02-03
IOQ11995-07-31

PMN#

GUDID#