Pentax Medical of America, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pentax Medical of America, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PENTAX Medical Video Colonoscope EC34-i10T Series, PENTAX Video Upper G.I. Scope EG34-i10
2
Total
2
Cleared
0
Denied
Pentax Medical of America, Inc. has 2 FDA 510(k) cleared medical devices. Based in Montvale, US.
Historical record: 2 cleared submissions from 2018 to 2018. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Pentax Medical of America, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pentax Medical of America, Inc.
2 devices