World of Medicine Lemke GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
World of Medicine Lemke GmbH - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
World of Medicine Lemke GmbH has 7 FDA 510(k) cleared medical devices. Based in Cambridge, US.
Historical record: 7 cleared submissions from 2002 to 2003. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by World of Medicine Lemke GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - World of Medicine Lemke GmbH
7 devices
Cleared
Mar 18, 2003
SIGHTFIX
General & Plastic Surgery
85d
Cleared
Jan 14, 2003
ENDOSCOPIC LIGHT SOURCE XL180/L3
Gastroenterology & Urology
90d
Cleared
Aug 20, 2002
ENDOSCOPIC LIGHT SOURCE, MODEL XL300/L5
Gastroenterology & Urology
89d
Cleared
Aug 01, 2002
ER150/M2
General & Plastic Surgery
87d
Cleared
Jun 05, 2002
ENDOSCOPIC LIGHT SOURCE XL202/L3
Gastroenterology & Urology
78d
Cleared
Mar 14, 2002
ENDOSCOPIC CAMERA TC804/C4
General & Plastic Surgery
85d
Cleared
Mar 14, 2002
ENDOSCOPIC CAMERA MC404/C3
General & Plastic Surgery
41d