Medicatech USA is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medicatech USA - FDA 510(k) Cleared Devices
Recent clearances: MasterX 800 Series, MasteRad MX30
9
Total
9
Cleared
0
Denied
Medicatech USA has 9 FDA 510(k) cleared medical devices. Based in Deer Field, US.
Last cleared in 2023. Active since 2008. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Medicatech USA Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kamm & Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Medicatech USA
9 devices
Cleared
Sep 01, 2023
MasterX 800 Series
Radiology
151d
Cleared
Apr 25, 2019
MasteRad MX30
Radiology
48d
Cleared
Feb 06, 2015
KrystalRad 11000 and KrystalRad 3000 Digital Stationary Radiographic System
Radiology
85d
Cleared
May 17, 2013
KRYSTALRAD NEW SERIESDIGITAL RADIOGRAPHIC PORTABLE RETROFIT SYSTEM
Radiology
92d
Cleared
Nov 18, 2011
KRYSTALRAD 660 DIGITAL RADIOGRAPHIC PORTABLE RETROFIT SYSTEM
Radiology
115d
Cleared
Jan 03, 2011
KRYSTALRAD 560 (FLAATZ 560)
Radiology
144d
Cleared
Jan 03, 2011
KRYSTALRAD (ATAL8)
Radiology
144d
Cleared
Oct 28, 2008
DIGITAL DIAGNOSTIC X-RAY SYSTEM, MODELS MAK 1500, MAK 2000 AND MAK 3000
Radiology
35d
Cleared
May 15, 2008
MEDICATECH, MODEL DDR MAK-800, DDT MAK-1000 FS, DDR MAK-1100 FA
Radiology
73d