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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
Website
www.peregrinesurgical.com
LinkedIn
—
Facebook
—
Email
[email protected]
Phone
2153480456
PRRC Contact
Melissa DeHass
EUDAMED SRN
US-MF-000002263
FDA FEI Number
1000121498
DUNS Number
—

Catalogue (237)

Page 5 of 5
DeviceModel / ReferenceRegistriesClassStatus
20GA Hard Tip Aspirating Laser Probe - Iridex PD720.62HT
FDA UDI
Class IIActive
25GA Membrane Scraper 1290.S25-00
FDA UDI
Class IActive
20GA Soft Tip Aspirating Laser Probe - Alcon PD720.60
FDA UDI
Class IIActive
25GA Curved Illuminating Laser Probe 7625.ALCU
FDA UDI
Class IIActive
20GA Curved Laser Probe - HGM PD720.21
FDA UDI
Class IIActive
25GA Curved Alcon Illuminating Laser Probe - Alcon PD725.35A
FDA UDI
Class IIActive
25GA Light Pipe - B&L PD126.25
FDA UDI
Class IIActive
25GA Midfield Endoillumination Probe 3269.M05-00
FDA UDI
Class IIActive
20GA Wide Angle Light Pipe - DORC PD104.09
FDA UDI
Class IIActive
23GA Illuminating Laser Probe, SMA906 GA-0040017
FDA UDI
Class IIActive
23GA Soft Tip Cannula PD223.00
FDA UDI
Class IActive
20GA Light Pipe - 287 Connector PD101.00
FDA UDI
Class IIActive
25GA Flexible 41GA Cannula 1270.05-00
FDA UDI
Class IActive
23GA Forceps - Sterile PD423.00S
FDA UDI
Class IActive
23GA Illuminating Laser Probe, SMA905 GA-0040004
FDA UDI
Class IIActive
23GA Illuminating Laser Probe, SMA905 GA-0040075
FDA UDI
Class IIActive
25GA Curved Illuminating Probe, SMA906 GA-0040018
FDA UDI
Class IIActive
Peregrine Fiber Optic Multi-Function Manipulator K980797
FDA 510(k)
Class IIActive
Peregrine Soft Tip Aspirating Laser Probe, Model Pd720.60 K061024
FDA 510(k)
Class IIActive
Peregrine Pic Minipulator K940392
FDA 510(k)
Class IActive
Midfield Light Pipe, 23ga (3269.M06-00); Midfield Light Pipe, 25ga (3269.M05-00); Midfield Light Pipe, 27ga (3269.M04-00) K233653
FDA 510(k)
Class IIActive
Peregrine Reverse Cutting Knife Light Pipe K940391
FDA 510(k)
Class IIActive
Peregrine Optiport Vitrectomy Probe Model Pd500.20 K980399
FDA 510(k)
Class IIActive
Pvrs-Peregrine Vitreoretinal Scissor Model Pd505.10 K980400
FDA 510(k)
Class IIActive
Peregrine Illuminating Laser Probe Model Pd600.10 K031023
FDA 510(k)
Class IIActive
Peregrine Shielded Diffusion Probe K980027
FDA 510(k)
Class IIActive
23ga Curved Illuminating Laser Probe K122997
FDA 510(k)
Class IIActive
Peregrine Diffusion Light Pipe K950529
FDA 510(k)
Class IIActive
Peregrine Wide Angle Light Pipe K940393
FDA 510(k)
Class IIActive
Peregrine Wet Set, Model Pd400.00 K990518
FDA 510(k)
Class IIActive
Peregrine 23ga Curved Laser Probe K122905
FDA 510(k)
Class IIActive
Peregrine Fiber Optic Bipolar Straight Pick And Angled Pick, Models Pd100.12 And Pd100.13 K980530
FDA 510(k)
Class IIActive
Peregrine Curved Illuminating Laser Probe K132614
FDA 510(k)
Class IIActive
Peregrine Tapered Diffusion Probe K980025
FDA 510(k)
Class IIActive
V.f.i.-Viscous Fluid Infusion Tubing Set K981907
FDA 510(k)
Class IIActive
23ga Chandelier Illuminator, 25ga Chandelier Illuminator K151604
FDA 510(k)
Class IIActive
Peregrine Straight Laser Probe, Model Pd6000.00 K024061
FDA 510(k)
Class IIActive

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Authorities

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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