Soring GmbH Medizintechnik is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Soring GmbH Medizintechnik - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Soring GmbH Medizintechnik has 7 FDA 510(k) cleared medical devices. Based in Denton, US.
Historical record: 7 cleared submissions from 1999 to 2010. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Soring GmbH Medizintechnik Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Soring GmbH Medizintechnik
7 devices
Cleared
Apr 16, 2010
SORING MBC200/BCC140
General & Plastic Surgery
154d
Cleared
Oct 07, 2005
SORING GMBH SONOCA LIPO
General & Plastic Surgery
58d
Cleared
Jan 17, 2003
CPC BY SORING GMBH
General & Plastic Surgery
14d
Cleared
Jan 08, 2003
MBC SERIES
General & Plastic Surgery
30d
Cleared
Nov 13, 2001
SORING GMBH SONOCA 180/190
General & Plastic Surgery
89d
Cleared
Oct 22, 1999
SORING GMBH, ARCO 3000, ARCO 2000, ARCO 1000, MBC 601, MBC 600
General & Plastic Surgery
23d
Cleared
Sep 23, 1999
SORING GMBH, SONOCA 300
General & Plastic Surgery
99d