Konica Minolta Healthcare Americas, Inc. is one of 16101 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Konica Minolta Healthcare Americas, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Universal 1417PI, OTC DDR, Universal DR 1748
6
Total
6
Cleared
0
Denied
Konica Minolta Healthcare Americas, Inc. has 6 FDA 510(k) cleared medical devices. Based in Garner, US.
Latest FDA clearance: Jun 2026. Active since 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Konica Minolta Healthcare Americas, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by MEDIcept, Inc. and Kamm & Associates.
FDA 510(k) Regulatory Record - Konica Minolta Healthcare Americas, Inc.
6 devices
Cleared
Jun 12, 2026
Universal 1417PI
Radiology
267d
Cleared
Jul 27, 2022
OTC DDR
Radiology
30d
Cleared
Jan 21, 2022
Universal DR 1748
Radiology
29d
Cleared
Jan 12, 2022
Straight Arm DDR
Radiology
21d
Cleared
Dec 10, 2021
EXA
Radiology
353d
Cleared
Jan 15, 2020
KDR AU-DDR System Advanced U-Arm with Dynamic Digital Radiography, KDR AU...
Radiology
54d