FDA.reportPublic FDA data

PROMEDTEK, INC.

Matched from indexed company URL: PROMEDTEK INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30071349233007134923PROMEDTEK, INC.1N2026-01-0115475 N Greenway Hayden Loop Ste 21-22b Scottsdale AZ US 85260

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
00850886008009Replexa+ Device - Replexa+ Model C1416 Shortwave Diathermy Device8663882410info@promedtek.com
00850886008016Replexa+ Treatment Applicator - Replexa+ Model C1416 Shortwave Diathermy Treatment Applicator8663882410info@promedtek.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
912061264343771K162240ProMedTek Model C1400 Shortwave Diathermy DeviceIMJ2016-11-17

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
IMJ22016-11-17

PMN#

GUDID#