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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 4 of 5

Device	Model / Reference	Registries	Class	Status
23GA Curved Illuminating Probe, SMA905	GA-0040073	FDA UDI	Class II	Active
20GA Straight Laser Probe - Iridex	PD720.12	FDA UDI	Class II	Active
25GA Sheilded Wide Angle Light Pipe - Universal	PD125.14S	FDA UDI	Class II	Active
23GA Curved Alcon Illuminating Laser Probe - Alcon	PD723.35A	FDA UDI	Class II	Active
20GA Ryan Pick	PD100.07	FDA UDI	Class II	Active
20GA Illuminating Laser Probe - Iridex	PD720.32	FDA UDI	Class II	Active
20GA Side Irrigating Light Pipe	PD100.01	EUDAMEDFDA UDI	Class II	Active
23GA Illuminating Laser Probe, SMA906	GA-0040101	FDA UDI	Class II	Active
23GA Light Pipe - Universal	PD100.23	FDA UDI	Class II	Active
23GA Hard Tip Aspirating Laser Probe - Alcon	PD723.60HT	FDA UDI	Class II	Active
23GA Straight Laser Probe - Iridex - Short	PD723.12S	FDA UDI	Class II	Active
25GA Curved Alcon Illuminating Laser Probe - Alcon - Short	PD725.35SA	FDA UDI	Class II	Active
25GA Illuminating Laser Probe - Iridex - Short	PD725.32S	FDA UDI	Class II	Active
23GA Light Pipe - Grieshaber	PD103.23	FDA UDI	Class II	Active
20GA Multi-Function Manipulator - 297 Connector	PD102.11	FDA UDI	Class II	Active
20GA Alcon Illuminating Laser Probe - Iridex	PD720.32A	FDA UDI	Class II	Active
25GA Curved Illuminating Probe, SMA906	GA-0040103	FDA UDI	Class II	Active
23GA Curved Illuminating Laser Probe - Iridex - Short	PD723.37S	FDA UDI	Class II	Active
20GA Illuminating Laser Probe, SMA905	GA-0042190	FDA UDI	Class II	Active
25GA Wide Angle Light Pipe - Universal	PD125.14	FDA UDI	Class II	Active
23GA Bipolar Pick - Alcon	PD123.13	FDA UDI	Class II	Active
23GA Soft Tip Aspirating Laser Probe - Iridex	PD723.62	FDA UDI	Class II	Active
23GA Membrane Scraper	PD800.23	FDA UDI	Class I	Active
25GA Curved Illuminating Probe, SMA905	GA-0040005	FDA UDI	Class II	Active
25GA Forceps - Sterile	PD425.00S	FDA UDI	Class I	Active
23GA Flexible Membrane Scraper	PD800.23SF	FDA UDI	Class I	Active
25GA Curved Illuminating Laser Probe - Alcon - Short	PD725.35S	FDA UDI	Class II	Active
20GA Bipolar Pick - Universal	PD100.13	FDA UDI	Class II	Active
20GA Curved Laser Probe - Iridex	PD720.22	FDA UDI	Class II	Active
23GA Forceps - Non-Sterile	PD423.00	FDA UDI	Class I	Active
23GA Curved Laser Probe - Iridex	PD723.22	FDA UDI	Class II	Active
20GA Aspirating Laser Probe, SMA905	GA-0040000	FDA UDI	Class II	Active
23GA Curved Illuminating Probe, SMA905	GA-0042240	FDA UDI	Class II	Active
25GA Curved Laser Probe - Alcon - Short	PD725.20S	EUDAMEDFDA UDI	Class II	Active
20GA Curved Laser Probe, SMA906	GA-0040015	FDA UDI	Class II	Active
27GA Straight Laser Probe - Iridex	PD727.12	FDA UDI	Class II	Active
25GA Illuminating Laser Probe, SMA906	GA-0040019	FDA UDI	Class II	Active
Vitrectomy Infusion Sleeve - Non-Sterile	PD505.05	FDA UDI	Class I	Active
25GA Flexible 41GA Cannula	PD225.41	FDA UDI	Class I	Active
25GA Membrane Scraper	PD800.25	FDA UDI	Class I	Active
20GA Straight Laser Probe, SMA905	GA-0042170	FDA UDI	Class II	Active
20GA Curved Illuminating Probe, SMA 905	GA-0040011	FDA UDI	Class II	Active
DMEK Infusion Sleeve	PD500.27	FDA UDI	Class I	Unknown
20GA Light Pipe - DORC	PD104.00	FDA UDI	Class II	Active
23GA Light Pipe - B&L	PD101.23	FDA UDI	Class II	Active
20GA Forceps - Sterile	PD420.00S	FDA UDI	Class I	Active
25GA Curved Alcon Illuminating Laser Probe - Iridex	PD725.37A	FDA UDI	Class II	Active
25GA Light Pipe - Universal	PD125.25	FDA UDI	Class II	Active
25GA Illuminating Laser Probe, SMA905	GA-0042270	FDA UDI	Class II	Active
20GA Straight Laser Probe - Alcon	PD720.10	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