Applied Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Applied Medical - FDA 510(k) Cleared Devices
Recent clearances: Voyant Fine Fusion Device (EB230), GelPOINT Mini Advanced Access Platform
14
Total
14
Cleared
0
Denied
Applied Medical has 14 FDA 510(k) cleared general & plastic surgery devices. Based in Fort Worth, US.
Last cleared in 2021. Active since 1985.
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 - Applied Medical
14 devices
Cleared
Dec 16, 2021
Voyant Fine Fusion Device (EB230)
General & Plastic Surgery
448d
Cleared
Apr 29, 2020
GelPOINT Mini Advanced Access Platform
General & Plastic Surgery
292d
Cleared
Oct 02, 2012
EPIX IRRIGATION PUMP, EPIX SUCTION IRRIGATION TUBING SET
General & Plastic Surgery
35d
Cleared
Oct 23, 2007
EXPANDING VASCULAR SHEATH
Cardiovascular
208d
Cleared
Feb 01, 2001
SUCTION IRRIGATOR
Gastroenterology & Urology
87d
Cleared
Jan 08, 2001
FLEXIBLE OCCLUSION SYSTEM
Cardiovascular
112d
Cleared
Jun 02, 1992
BIO-POLAR FORCEPS
General & Plastic Surgery
155d
Cleared
Apr 22, 1991
SURGICAL TROCAR
Cardiovascular
19d
Cleared
Apr 01, 1985
APPLIED GAUZE SPONGE 4X4X16 PLY
General & Plastic Surgery
122d
Cleared
Apr 01, 1985
APPLIED GAUZE SPONGE 2X2X8 PLY
General & Plastic Surgery
122d
Cleared
Apr 01, 1985
APPLIED GAUZE SPONGE 3X3X12
General & Plastic Surgery
122d
Cleared
Apr 01, 1985
APPLIED GAUZE SPONGE 4X4X8
General & Plastic Surgery
122d