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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 3 of 5

Device	Model / Reference	Registries	Class	Status
20GA Straight Pick	PD100.03	FDA UDI	Class II	Active
25GA Soft Tip Cannula - 1mm Silicone	PD225.01	FDA UDI	Class I	Active
23GA Straight Laser Probe - Alcon - Short	PD723.10S	FDA UDI	Class II	Active
25GA Flexible Membrane Scraper	PD800.25SF	FDA UDI	Class I	Active
25GA Curved Illuminating Laser Probe - Short	PD725.37SDD	FDA UDI	Class II	Active
23GA Straight Laser Probe - Iridex	PD723.12	FDA UDI	Class II	Active
DMEK/DSAEK Infusion Sleeve	PD500.27	FDA UDI	Class I	Unknown
23GA Alcon Illuminating Laser Probe - Iridex	PD723.32A	FDA UDI	Class II	Active
20GA Tapered Diffusion Light Pipe - Standard	PD103.14	FDA UDI	Class II	Active
20GA Non-Adjustable Membrane Scraper	PD800.20	FDA UDI	Class I	Active
20GA Ryan Pick - 287 Connector	PD101.07	FDA UDI	Class II	Active
20GA Curved Illuminating Probe, SMA906	GA-0040115	FDA UDI	Class II	Active
20GA Curved Alcon Illuminating Laser Probe - Alcon	PD720.35A	FDA UDI	Class II	Active
20GA Membrane Scraper	PD800.00	FDA UDI	Class I	Active
27GA Midfield Endoillumination Probe	3269.M04-00	FDA UDI	Class II	Active
23GA Straight Laser Probe, SMA905	GA-0042210	FDA UDI	Class II	Active
25GA Illuminating Laser Probe - Alcon	PD725.30	FDA UDI	Class II	Active
23GA Flexible 41GA Cannula	PD223.41	FDA UDI	Class I	Active
20GA Curved Alcon Illuminating Laser Probe - Iridex	PD720.37A	FDA UDI	Class II	Active
23GA Curved Illuminating Probe, SMA906	GA-0040099	FDA UDI	Class II	Active
20GA Tapered Diffusion Light Pipe - 287 Connector	PD101.14	EUDAMEDFDA UDI	Class II	Active
25GA Straight Laser Probe - Iridex - Short	PD725.12S	FDA UDI	Class II	Active
25GA Illuminating Laser Probe, SMA906	GA-0040105	FDA UDI	Class II	Active
23GA Illuminating Laser Probe, SMA905	GA-0042230	FDA UDI	Class II	Active
20GA Curved Illuminating Probe, SMA906	GA-0040024	FDA UDI	Class II	Active
20GA Illuminating Laser Probe, SMA906	GA-0040113	FDA UDI	Class II	Active
20GA Bipolar Manipulator - Standard	PD103.12	FDA UDI	Class II	Active
20GA Illuminating Laser Probe - Alcon	PD720.30	FDA UDI	Class II	Active
25GA Illuminating Laser Probe - Iridex	PD725.32	FDA UDI	Class II	Active
25GA Straight Laser Probe, SMA906	GA-0040021	FDA UDI	Class II	Active
23GA Light Pipe - Alcon	PD102.23	FDA UDI	Class II	Active
20GA Curved Laser Probe - Alcon	PD720.20	FDA UDI	Class II	Active
20GA Bipolar Manipulator	PD100.12	FDA UDI	Class II	Active
20GA Sheilded Wide Angle Light Pipe - Universal (Large)	PD100.14S	FDA UDI	Class II	Active
DMEK/DSAEK Forceps	PD427.00	FDA UDI	Class I	Active
25GA Soft Tip Cannula - 1mm Silicone	1272.SD125-00	FDA UDI	Class I	Active
25GA Illuminating Laser Probe - Alcon - Short	PD725.30S	FDA UDI	Class II	Active
23GA Straight Laser Probe - Alcon	PD723.10	FDA UDI	Class II	Active
20GA Wide Angle Light Pipe	PD100.09	FDA UDI	Class II	Active
Monofilament, Fine	PD100.06	FDA UDI	Class II	Active
20GA Wide Angle Light Pipe - 287 Connector	PD101.09	FDA UDI	Class II	Active
23GA Illuminating Laser Probe - Iridex - Short	PD723.32S	FDA UDI	Class II	Active
25GA Forceps - Non-Sterile	PD425.00	FDA UDI	Class I	Active
20GA Curved Illuminating Laser Probe - Iridex	PD720.37	FDA UDI	Class II	Active
20GA Soft Tip Cannula	PD220.00	FDA UDI	Class I	Active
20GA Soft Tip Aspirating Laser Probe - Iridex	PD720.62	FDA UDI	Class II	Active
Dugel Entry Plate	PD490.23	FDA UDI	Class I	Active
20GA 1mm Bipolar Pick - Universal	PD100.15	FDA UDI	Class II	Active
27GA Curved Illuminating Laser Probe - Iridex	7627.IRI-00	FDA UDI	Class II	Active
25GA Alcon Illuminating Laser Probe - Alcon	PD725.30A	FDA UDI	Class II	Active

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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.

Date	Recall No.	Class	Status	Reason
Jul 19, 2010	Z-2399-2010	—	terminated	Product did not have proper 510(k) clearance