Peregrine Surgical , Ltd. is one of 9816 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Peregrine Surgical , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: 23ga Chandelier Illuminator, 25ga Chandelier Illuminator, PEREGRINE CURVED ILLUMINATING LASER PROBE, 23GA CURVED ILLUMINATING LASER PROBE
19
Total
19
Cleared
0
Denied
Peregrine Surgical , Ltd. has 19 FDA 510(k) cleared ophthalmic devices. Based in Doylestown, US.
Historical record: 19 cleared submissions from 1994 to 2015.
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 - Peregrine Surgical , Ltd.
19 devices
Cleared
Sep 11, 2015
23ga Chandelier Illuminator, 25ga Chandelier Illuminator
Ophthalmic
88d
Cleared
Nov 14, 2013
PEREGRINE CURVED ILLUMINATING LASER PROBE
Ophthalmic
85d
Cleared
Jun 26, 2013
23GA CURVED ILLUMINATING LASER PROBE
Ophthalmic
272d
Cleared
Apr 30, 2013
PEREGRINE 23GA CURVED LASER PROBE
Ophthalmic
221d
Cleared
Jun 21, 2006
PEREGRINE SOFT TIP ASPIRATING LASER PROBE, MODEL PD720.60
Ophthalmic
69d
Cleared
Jun 27, 2003
PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10
Ophthalmic
88d
Cleared
Mar 07, 2003
PEREGRINE STRAIGHT LASER PROBE, MODEL PD6000.00
General & Plastic Surgery
88d
Cleared
Mar 25, 1999
PEREGRINE WET SET, MODEL PD400.00
General Hospital
35d
Cleared
Aug 04, 1998
V.F.I.-VISCOUS FLUID INFUSION TUBING SET
Ophthalmic
64d
Cleared
May 19, 1998
PEREGRINE FIBER OPTIC MULTI-FUNCTION MANIPULATOR
Ophthalmic
78d
Cleared
May 12, 1998
PEREGRINE FIBER OPTIC BIPOLAR STRAIGHT PICK AND ANGLED PICK, MODELS PD100.12...
Ophthalmic
90d
Cleared
Apr 30, 1998
PEREGRINE OPTIPORT VITRECTOMY PROBE MODEL PD500.20
Ophthalmic
87d