Tissuelink Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tissuelink Medical, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Tissuelink Medical, Inc. has 12 FDA 510(k) cleared general & plastic surgery devices. Based in Dover, US.
Historical record: 12 cleared submissions from 2000 to 2008.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tissuelink Medical, Inc.
12 devices
Cleared
Jan 09, 2008
TISSUELINK AQUAMANTYS MALLEABLE BIPOLAR SEALER WITH LIGHT
General & Plastic Surgery
28d
Cleared
Feb 22, 2007
AQUAMANTYS SS4.0 BIPOLAR SEALER, MODEL 23-121-1
General & Plastic Surgery
77d
Cleared
Oct 25, 2005
AQUAMANTYS PUMP GENERATOR SYSTEM
General & Plastic Surgery
14d
Cleared
Aug 20, 2003
TISSUELINK FLOATING BALL MODEL 23-201-1
General & Plastic Surgery
40d
Cleared
Mar 03, 2003
TISSUELINK SEALING FORCEPS, MODEL 1 21-202-1
General & Plastic Surgery
26d
Cleared
Feb 12, 2003
TISSUELINK BIPOLAR FLOATING BALL DEVICE
General & Plastic Surgery
196d
Cleared
May 20, 2002
TISSUELINK BIPOLAR FLOATING BALL DEVICE
General & Plastic Surgery
88d
Cleared
Mar 27, 2002
TISSUELINK SOLID CYLINDER MONOPOLAR DEVICE
General & Plastic Surgery
90d
Cleared
May 03, 2001
MODIFICATION TO TISSUELINK BIPOLAR FORCEPS
General & Plastic Surgery
63d
Cleared
Apr 27, 2001
MODIFICATION TO TISSUELINK MONOPOLAR FLOATING BALL
General & Plastic Surgery
57d
Cleared
Dec 08, 2000
TISSUELINK BIPOLAR FORCEPS
General & Plastic Surgery
73d
Cleared
Nov 13, 2000
TISSUELINK MONOPOLAR FLOATING BALL'
General & Plastic Surgery
77d