Xomed, Inc. - FDA 510(k) Cleared Devices
82
Total
81
Cleared
0
Denied
Xomed, Inc. has 81 FDA 510(k) cleared medical devices. Based in Arnold, US.
Historical record: 81 cleared submissions from 1976 to 2000. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Xomed, Inc. Filter by specialty or product code using the sidebar.
82 devices
Cleared
Dec 11, 2000
MODEL 30 CLASSIC PNEUMATONOMETER
Ophthalmic
126d
Cleared
Dec 04, 2000
REDTRONIC XOMED MONOPOLAR ENERGIZED BLADE
General & Plastic Surgery
70d
Cleared
Oct 17, 2000
XPS NITRO SYSTEM
Ear, Nose, Throat
36d
Cleared
Oct 11, 2000
TITANIUM MIDDLE EAR PROSTHESES
Ear, Nose, Throat
23d
Cleared
Jun 09, 2000
MICRO-FRANCE TROCARS AND ACCESSORIES
Obstetrics & Gynecology
224d
Cleared
Jun 03, 2000
MEROGEL OTOLOGIC PACK
Ear, Nose, Throat
54d
Cleared
Feb 08, 2000
FRONTAL SINUS TREPHINATION CANNULA
General & Plastic Surgery
53d
Cleared
Jan 21, 2000
XPS STRAIGHTSHOT OR MODEL 2000 MICRODEBRIDER SYSTEM OR XPS POWERSCULPT
General & Plastic Surgery
150d
Cleared
Jan 20, 2000
MODIFICATION TO LASER-SHIELD II
Anesthesiology
90d
Cleared
Dec 21, 1999
MICRO-FRANCE ELECTROSURGICAL INSTRUMENTS, VARIOUS
General & Plastic Surgery
53d
Cleared
Dec 09, 1999
XOMED ENT RF SYSTEM
General & Plastic Surgery
83d
Cleared
Oct 07, 1999
XOMED BALL-TIP MONOPOLAR STIMULATOR PROBE
Ear, Nose, Throat
43d
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