MEDA Co., Ltd. is one of 16079 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
MEDA Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: MD-6000S Bladder Scanner, MD-320W Ultrasound Biomicroscope, MD-6000P Bladder Scanner
6
Total
6
Cleared
0
Denied
MEDA Co., Ltd. has 6 FDA 510(k) cleared medical devices. Based in Potomac, US.
Latest FDA clearance: Sep 2026. Active since 2012. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by MEDA Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Meditech International, Inc. and Medtech International, Inc..
FDA 510(k) Regulatory Record - MEDA Co., Ltd.
6 devices
Cleared
Sep 24, 2026
MD-6000S Bladder Scanner
Radiology
237d
Cleared
Nov 18, 2021
MD-320W Ultrasound Biomicroscope
Radiology
56d
Cleared
May 06, 2019
MD-6000P Bladder Scanner
Radiology
238d
Cleared
Nov 17, 2015
MD-2300S Ultrasonic A/B Scanner for Ophthalmology
Radiology
92d
Cleared
May 03, 2013
ULTRASONIC BIOMETER FOR OPHTHALMOLOGY ULTRASONIC PACHYMETER
Radiology
373d
Cleared
Mar 23, 2012
BLADDER SCANNER
Radiology
136d