Grieshaber & Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Grieshaber & Co. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Grieshaber & Co. has 15 FDA 510(k) cleared medical devices. Based in Fallisington, US.
Historical record: 15 cleared submissions from 1986 to 1995. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Grieshaber & Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Grieshaber & Co.
15 devices
Cleared
May 05, 1995
THE GRIESHABER AXIAL CUTTER
Ophthalmic
119d
Cleared
May 03, 1994
THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGE
Ophthalmic
440d
Cleared
Jun 11, 1992
GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGE
General & Plastic Surgery
239d
Cleared
Jan 23, 1992
GRIESHABER AIR/FLUID TUBING SET
Ophthalmic
99d
Cleared
Jan 03, 1992
GRIESHABER TWO FUNCTION MANIPULATOR
Ear, Nose, Throat
79d
Cleared
Jan 03, 1992
GRIESHABER THREE FUNCTION MANIPULATOR
Ear, Nose, Throat
79d
Cleared
Apr 12, 1990
GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP
Ophthalmic
107d
Cleared
Mar 27, 1990
ZZIPP INSTANT BOVIE CLEANER
General & Plastic Surgery
41d
Cleared
Jun 23, 1989
GRIESHABER SOFT TIP NEEDLE (20 & 19 GAUGES)
Ophthalmic
128d
Cleared
May 16, 1989
GRIESHABER VISCOELASTIC INJECTION SYSTEM
General Hospital
90d
Cleared
Nov 16, 1988
GRIESHABER MICRO LITE LIGHT PIPE 19 & 20 GAUGE
Ophthalmic
51d
Cleared
Oct 31, 1986
GRIESHABER GLOBAL CONTROL TUBING SET
Ophthalmic
53d