Oculo Plastik, Inc. is one of 204 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Oculo Plastik, Inc. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Oculo Plastik, Inc. has 13 FDA 510(k) cleared ophthalmic devices. Based in Montreal, Quebec Canada, CA.
Historical record: 13 cleared submissions from 1990 to 2013.
Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Oculo Plastik, Inc. — FDA 510(k) Products and Clearance History
13 devices
Cleared
Jan 31, 2013
DURETTE OCULAR IMPLANT
Ophthalmic
55d
Cleared
Sep 15, 2011
SILICONE SPHERES
Ophthalmic
49d
Cleared
Mar 19, 2008
DURETTE IMPLANT
Ophthalmic
117d
Cleared
Jun 10, 2004
EYE SPHERE IMPLANTS
Ophthalmic
86d
Cleared
May 05, 1994
EPTFE SHEET COVERING FOR OCULAR IMPLANT
Ophthalmic
209d
Cleared
Mar 02, 1992
OPHTIMPLANT
Ophthalmic
76d
Cleared
May 22, 1990
O'DONNELL, SOCKET RECONSTRUCTION PROSTHESES
Ophthalmic
81d
Cleared
May 18, 1990
PUTTERMAN-SCOTT, SOCKET RECONSTRUCTION BILATERAL
Ophthalmic
80d
Cleared
May 15, 1990
CODERE-DURETTE ORBITAL FLOOR IMPLANT
Ophthalmic
77d
Cleared
May 15, 1990
COX MALAR EMINENCE IMPLANTS
Ophthalmic
77d
Cleared
May 15, 1990
SPIVEY-ALLEN ORBITAL FLOOR IMPLANT
Ophthalmic
77d
Cleared
Mar 23, 1990
NEW IOWA MOTILITY IMPLANT
Ophthalmic
78d
Cleared
Mar 23, 1990
NEW ALLEN IMPLANT
Ophthalmic
78d