Dornier Medtech America, Inc. - FDA 510(k) Cleared Devices
40
Total
40
Cleared
0
Denied
Dornier Medtech America, Inc. has 40 FDA 510(k) cleared medical devices. Based in Marietta, US.
Last cleared in 2023. Active since 1990. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Dornier Medtech America, Inc. Filter by specialty or product code using the sidebar.
40 devices
Cleared
Feb 22, 2023
Delta III Pro
Gastroenterology & Urology
237d
Cleared
Jul 27, 2022
Dornier Thulio
Gastroenterology & Urology
300d
Cleared
Apr 18, 2022
Nautilus
Radiology
24d
Cleared
May 19, 2021
Electrosurgical accessory
Gastroenterology & Urology
98d
Cleared
Nov 20, 2020
Dornier MAGELLAN Ureteral Access Sheath
Gastroenterology & Urology
142d
Cleared
Sep 03, 2020
Delta III Lithotripter
Gastroenterology & Urology
134d
Cleared
Dec 06, 2019
EQUINOX Balloon Dilatation Catheter
Gastroenterology & Urology
270d
Cleared
Nov 15, 2019
Dornier Ureteral Stent
Gastroenterology & Urology
276d
Cleared
Sep 18, 2019
Dornier MINNOW Ureteral Catheter
Gastroenterology & Urology
138d
Cleared
Aug 08, 2017
Delta III Lithotripter
Gastroenterology & Urology
29d
Cleared
Jul 28, 2016
Medilas H Laser Fibers
General & Plastic Surgery
30d
Cleared
Oct 08, 2015
Medilas H RFID Laser Fibers
General & Plastic Surgery
28d
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