Lacrimedics, Inc. is one of 11825 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lacrimedics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: COLLASYN PLUG FOR THE LACRIMAL EFFICIENCY TEST, HERRICK ULTIMATE PUNCTUM PLUG, HERRICK ULTIMATE PUNCTUM PLUG
12
Total
12
Cleared
0
Denied
Lacrimedics, Inc. has 12 FDA 510(k) cleared ophthalmic devices. Based in San Marino, US.
Historical record: 12 cleared submissions from 1985 to 2016.
Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lacrimedics, Inc.
12 devices
Cleared
Nov 18, 2016
LacriPro Punctum Plug
Ophthalmic
155d
Cleared
Jun 03, 2014
COLLASYN PLUG FOR THE LACRIMAL EFFICIENCY TEST
Ophthalmic
148d
Cleared
May 09, 2003
OPAQUE HERRICK LACRIMAL PLUG
Ophthalmic
100d
Cleared
Jul 01, 2002
OPAQUE HERRICK LACRIMAL PLUG, 0.3MM,0.5MM,0.7MM, MODELS...
Ophthalmic
27d
Cleared
Jun 19, 2000
OPAQUE HERRICK PLUG, 0.3MM
Ophthalmic
12d
Cleared
Apr 14, 1997
HERRICK ULTIMATE PUNCTUM PLUG
Ophthalmic
223d
Cleared
Apr 14, 1997
HERRICK ULTIMATE PUNCTUM PLUG
Ophthalmic
210d
Cleared
Nov 22, 1994
FOCOMETER
Ophthalmic
71d
Cleared
Jan 22, 1990
HERRICK LACRIMAL PLUG TM.
Ophthalmic
89d
Cleared
Nov 02, 1989
COLLAGEN IMPLANTS FOR THE LACRIMAL EFFICIENCY TEST
Ophthalmic
63d
Cleared
May 17, 1989
LACRIMAL EFFICIENCY TEST (TM)
Ophthalmic
93d
Cleared
May 21, 1985
ABSORBABLE INTRACANALICULAR COLLAGEN IMPLANT
Ophthalmic
91d