Dornier Medtech America, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dornier Medtech America, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Delta III Pro, Dornier Thulio, Nautilus
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.
FDA 510(k) Regulatory Record - Dornier Medtech America, Inc.
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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