Ophthalmic Technologies, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Ophthalmic Technologies, Inc. - FDA 510(k) Cleared Devices
9
Total
8
Cleared
0
Denied
Ophthalmic Technologies, Inc. has 8 FDA 510(k) cleared medical devices. Based in Downsview, Ontario, CA.
Historical record: 8 cleared submissions from 1995 to 2005. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Ophthalmic Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ophthalmic Technologies, Inc.
9 devices
Cleared
Jan 21, 2005
OCT-OPTHALMOSCOPE
Ophthalmic
94d
Cleared
Jun 20, 2003
HF MODULE WITH TRANSDUCERS
Radiology
49d
Cleared
Mar 27, 2003
OTI SCAN WITH TRANSDUCERS
Radiology
16d
Cleared
Jan 10, 2003
A-SCAN 100
Radiology
28d
Cleared
Apr 04, 1999
DI-RHEX OPHTHALMIC DIATHERMY SYSTEM
Ophthalmic
86d
Cleared
Feb 25, 1998
3D I-SCAN
Radiology
85d
Cleared
Jun 25, 1997
I-SCOPE OPHTHALMIC ENDOSCOPE
Ophthalmic
49d
Cleared
May 13, 1996
I-SCAN
Radiology
90d
Cleared
Oct 18, 1995
XE-LITE
General & Plastic Surgery
36d