Summit Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Summit Technology, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Summit Technology, Inc. has 5 FDA 510(k) cleared medical devices. Based in Waltham, US.
Historical record: 5 cleared submissions from 1990 to 1998. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Summit Technology, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Summit Technology, Inc.
5 devices
Cleared
Dec 22, 1998
SUMMIT KRUMEICH-BARRAQUER MICROKERATOME
Ophthalmic
305d
Cleared
Jul 22, 1993
LASER AND EMPHASIS SCLEROSTOMY TIP
Ophthalmic
206d
Cleared
Jun 15, 1992
OMNIMED HOLMIUM LASER AND DELIVERY SYSTEM
General & Plastic Surgery
180d
Cleared
Jul 25, 1991
OMNIVIEW(TM) OPHTHALMIC FIBERENDO W/NEEDLEHOLDER
Ear, Nose, Throat
64d
Cleared
Dec 24, 1990
SUMMIT TECH 19/20 GAUGE OPHTHALMIC FIBERENDOSCOPE
Ear, Nose, Throat
84d