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Peregrine Surgical, LLC.

United States·US-MF-000002263

Last updated September 17, 2026

Information

Country
United States
Address
51, Britain Drive, NEW BRITAIN, United States
LinkedIn
—
Facebook
—
Phone
2153480456
PRRC Contact
Melissa DeHass
EUDAMED SRN
US-MF-000002263
FDA FEI Number
1000121498
DUNS Number
—

Catalogue (237)

Page 2 of 5
DeviceModel / ReferenceRegistriesClassStatus
25GA Alcon Illuminating Laser Probe - Iridex - Short PD725.32SA
FDA UDI
Class IIActive
20GA Tapered Diffusion Light Pipe - Universal (Large) PD100.14
FDA UDI
Class IIActive
23GA Curved Universal Illuminating Laser Probe - Alcon - PF PD723.35-PF
FDA UDI
Class IIActive
23GA Curved Alcon Illuminating Laser Probe - Alcon - PF PD723.35A-PF
FDA UDI
Class IIActive
25GA Straight Laser Probe - Alcon PD725.10
FDA UDI
Class IIActive
25GA Alcon Illuminating Laser Probe - Alcon - Short PD725.30SA
FDA UDI
Class IIActive
20GA Light Pipe PD100.00
FDA UDI
Class IIActive
25GA Curved Laser Probe - Iridex - Short PD725.22S
FDA UDI
Class IIActive
23GA Curved Alcon Illuminating Laser Probe - Alcon - Short PD723.35SA
FDA UDI
Class IIActive
23GA Soft Tip Cannula - 1mm Silicone PD223.01
FDA UDI
Class IActive
23GA Straight Pick PD123.03AD
FDA UDI
Class IIActive
23GA Sheilded Wide Angle Light Pipe - Universal PD123.14S
FDA UDI
Class IIActive
20GA Forceps - Non-Sterile PD420.00
FDA UDI
Class IActive
23GA Curved Laser Probe, SMA906 GA-0040014
FDA UDI
Class IIActive
DMEK/DSAEK Infusion Sleeve PD500.27
FDA UDI
Class IActive
25GA Straight Laser Probe - Alcon - Short PD725.10S
FDA UDI
Class IIActive
25GA Illuminating Laser Probe. SMA 905 GA-0040006
FDA UDI
Class IIActive
23GA Alcon Illuminating Laser Probe - Alcon PD723.30A
FDA UDI
Class IIActive
25GA Straight Lasr Probe - Iridex PD725.12
FDA UDI
Class IIActive
23GA Soft Tip Aspirating Laser Probe - Alcon PD723.60
FDA UDI
Class IIActive
20GA 45 Degree Pick - 287 Connector PD101.04
FDA UDI
Class IIActive
20GA 45 Degree Pick PD100.04
FDA UDI
Class IIActive
20GA 45 Degree Pick - 297 Connector PD102.04
FDA UDI
Class IIActive
23GA Straight Pick - Universal PD123.03
FDA UDI
Class IIActive
20GA Wide Angle Light Pipe - Standard PD103.09
FDA UDI
Class IIActive
23GA Wide Angle Light Pipe - Universal PD123.14
FDA UDI
Class IIActive
20GA Bipolar Manipulator - 297 Connector PD102.12
FDA UDI
Class IIActive
23GA Straight Pick - Alcon PD123.03A
FDA UDI
Class IIActive
23GA Curved Illuminating Probe, SMA906 GA-0040016
FDA UDI
Class IIActive
25GA Curved Illuminating Laser Probe - Iridex - Short PD725.37S
FDA UDI
Class IIActive
27GA Curved Laser Probe - Iridex PD727.22
FDA UDI
Class IIActive
23GA Curved Alcon Illuminating Laser Probe - Iridex - Short PD723.37SA
FDA UDI
Class IIActive
20GA Curved Laser Probe, SMA905 GA-0040002
FDA UDI
Class IIActive
20GA Illuminating Laser Probe, SMA905 GA-0040087
FDA UDI
Class IIActive
25GA Alcon Illuminating Laser Probe - Iridex PD725.32A
FDA UDI
Class IIActive
25GA Curved Laser Probe, SMA906 GA-0040020
FDA UDI
Class IIActive
25GA Illuminating Laser Probe, SMA905 GA-0040079
FDA UDI
Class IIActive
23GA Curved Laser Probe - Iridex - Short PD723.22S
FDA UDI
Class IIActive
23GA Curved Alcon Illuminating Laer Probe - Iridex PD723.37A
FDA UDI
Class IIActive
27GA Curved Illuminating Laser Probe - Alcon 7627.ALC-00
FDA UDI
Class IIActive
27GA Curved Laser Probe PD727.20DU
FDA UDI
Class IIActive
23GA Curved Laser Probe - Alcon - Short PD723.20S
FDA UDI
Class IIActive
DMEK/DSAEK Forceps PD427.00
FDA UDI
Class IUnknown
20GA Curved Illuminating Probe, SMA905 GA-0040089
FDA UDI
Class IIActive
23GA Membrane Scraper 1290.S23-00
FDA UDI
Class IActive
23GA Illuminating Laser Probe - Alcon - Short PD723.30S
FDA UDI
Class IIActive
20GA Curved Illuminating Laser Probe - Alcon PD720.35
FDA UDI
Class IIActive
23GA Curved Laser Probe, SMA905 GA-0042220
FDA UDI
Class IIActive
23GA Curved Illuminating Probe, SMA905 GA-0040003
FDA UDI
Class IIActive
20GA Wide Angle Light Pipe - 297 Connector PD102.09
FDA UDI
Class IIActive

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Authorised Representatives

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Importers

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Notified Bodies

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Authorities

Not available yet.

FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Jul 19, 2010Z-2399-2010—terminated

Product did not have proper 510(k) clearance