W.O.M. World of Medicine GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
W.O.M. World of Medicine GmbH - FDA 510(k) Cleared Devices
Recent clearances: PUREVUE™ FMS, PNEUMOCLEAR, ARTHRO-Pump PA304
26
Total
26
Cleared
0
Denied
W.O.M. World of Medicine GmbH has 26 FDA 510(k) cleared medical devices. Based in Tucson, US.
Latest FDA clearance: Dec 2025. Active since 1992. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by W.O.M. World of Medicine GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Susanne Raab as regulatory consultant.
FDA 510(k) Regulatory Record - W.O.M. World of Medicine GmbH
26 devices
Cleared
Dec 05, 2025
PUREVUE™ FMS
Orthopedic
266d
Cleared
Jul 29, 2020
PNEUMOCLEAR
Obstetrics & Gynecology
68d
Cleared
May 09, 2018
ARTHRO-Pump PA304
Orthopedic
203d
Cleared
Mar 28, 2018
GYN-Pump PH304
Obstetrics & Gynecology
135d
Cleared
Feb 05, 2018
Aquilex Fluid Control System AQL-100S
Obstetrics & Gynecology
215d
Cleared
May 15, 2017
PNEUMOCLEAR
Obstetrics & Gynecology
61d
Cleared
Mar 21, 2017
LAP-Pump PP110
Obstetrics & Gynecology
118d
Cleared
Mar 04, 2016
Insufflator 50L FM134
Obstetrics & Gynecology
88d
Cleared
Oct 13, 2015
HD-Camera HDC1000
Gastroenterology & Urology
76d
Cleared
Nov 01, 2001
W.O.M. LASER U100
General & Plastic Surgery
198d
Cleared
Feb 08, 2000
ARTHRO-SURGIMAT-A103
Orthopedic
21d
Cleared
Jul 23, 1999
LAP-WAVE 3000 (P07)
Obstetrics & Gynecology
140d