Origin Medsystems, Inc. - FDA 510(k) Cleared Devices
50
Total
49
Cleared
0
Denied
Origin Medsystems, Inc. has 49 FDA 510(k) cleared general & plastic surgery devices. Based in San Mateo, US.
Historical record: 49 cleared submissions from 1989 to 1999.
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.
50 devices
Cleared
Jul 30, 1999
BLUNT TIP TROCAR PORT
General & Plastic Surgery
16d
Cleared
May 29, 1998
VASOVIEW DISSECTION/VESSEL HARVESTING SYSTEM
General & Plastic Surgery
15d
Cleared
Oct 01, 1997
ORIGIN LIGATOR DEVICE
General & Plastic Surgery
76d
Cleared
Aug 19, 1997
ORIGIN CARDIAC STABLIZER OCCLUDER
Cardiovascular
182d
Cleared
Mar 20, 1997
CANNULA
Obstetrics & Gynecology
87d
Cleared
Feb 14, 1997
VASOVIEW BALLOON DISSECTION SYSTEM
General & Plastic Surgery
119d
Cleared
Sep 11, 1996
AIRLIFT BALLOON RETRACTON SYSTEM
General & Plastic Surgery
104d
Cleared
Aug 12, 1996
EXTRAHAND BALLOON RETRACTOR
General & Plastic Surgery
82d
Cleared
Jul 24, 1996
RESPOSABLE TROCAR SYSTEM [5MM, 5MM SHORT, 10MM AND 12MM SIZES]
Obstetrics & Gynecology
138d
Cleared
Jun 14, 1996
5MM ENDOSCOPE
General & Plastic Surgery
121d
Cleared
Jan 24, 1996
DISSECTION PROBE
General & Plastic Surgery
72d
Cleared
Nov 09, 1995
DUO BALLOON SYSTEM (DBS) 2 [10 AND 12 MM SIZES]
General & Plastic Surgery
65d
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