FDA.reportPublic FDA data

MEDICATECH USA

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30049898043004989804MEDICATECH USA1N2026-01-011245 N Patt St Anaheim CA US 92801

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
00860001404753MasteRad - MasteRad MX-30 Radiographic System+1 949-679-2881info@medicatechusa.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
651561289838252K230918MasterX 800 SeriesMQB2023-09-01
651561591143360K190601MasteRad MX30KPR2019-04-25
651561224742971K143257KrystalRad 11000 and KrystalRad 3000 Digital Stationary Radiographic SystemKPR2015-02-06
651561880923422K082798DIGITAL DIAGNOSTIC X-RAY SYSTEM, MODELS MAK 1500, MAK 2000 AND MAK 3000KPR2008-10-28
651561644558979K080582MEDICATECH, MODEL DDR MAK-800, DDT MAK-1000 FS, DDR MAK-1100 FAKPR2008-05-15
651561505887268
651561899541430

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
KPR42019-04-25
MQB12023-09-01

PMN#

GUDID#