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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 1 of 5

Device	Model / Reference	Registries	Class	Status
25GA Light Pipe - Grieshaber	PD128.25	FDA UDI	Class II	Active
23GA Curved Illuminating Laser Probe - Iridex	PD723.37	FDA UDI	Class II	Active
27GA Straight Laser Probe	PD727.10DU	FDA UDI	Class II	Active
23GA Curved Laser Probe, SMA905	GA-0040001	FDA UDI	Class II	Active
25GA Curved Illuminating Laser Probe - Alcon	PD725.35	FDA UDI	Class II	Active
25GA Light Pipe - Alcon	PD127.25	FDA UDI	Class II	Active
23GA Soft Tip Cannula - 1mm Silicone	1272.SD123-00	FDA UDI	Class I	Active
25GA Curved Laser Probe, SMA905	GA-0040007	FDA UDI	Class II	Active
23GA Curved Illuminating Laser Probe - Alcon - Short	PD723.35S	FDA UDI	Class II	Active
23GA Curved Illuminating Laser Probe - Alcon	PD723.35	FDA UDI	Class II	Active
DMEK Forceps	PD427.00	FDA UDI	Class I	Unknown
23GA Alcon Illuminating Laser Probe - Alcon - Short	PD723.30SA	FDA UDI	Class II	Active
Vitrectomy Infusion Sleeve	PD505.06	FDA UDI	Class I	Active
25GA Straight Laser Probe, SMA905	GA-0040008	FDA UDI	Class II	Active
23GA Illuminating Laser Probe - Iridex	PD723.32	FDA UDI	Class II	Active
20GA Illuminating Laser Probe, SMA905	GA-0040010	FDA UDI	Class II	Active
23GA Curved Universal Illuminating Laser Probe - Iridex - PF	PD723.37-PF	FDA UDI	Class II	Active
23GA Straight Laser Probe, SMA905	GA-0040009	FDA UDI	Class II	Active
20GA End Irrigating Light Pipe	PD100.02	FDA UDI	Class II	Active
23GA Curved Laser Probe - Alcon	PD723.20	FDA UDI	Class II	Active
23GA Alcon Illuminating Laser Probe - Iridex - Short	PD723.32SA	FDA UDI	Class II	Active
25GA Soft Tip Cannula	PD225.00	FDA UDI	Class I	Active
20GA Curved Laser Probe, SMA905	GA-0042180	FDA UDI	Class II	Active
25GA Curved Laser Probe - Alcon	PD725.20	FDA UDI	Class II	Active
23GA Hard Tip Aspirating Laser Probe - Iridex	PD723.62HT	FDA UDI	Class II	Active
25GA Straight Laser Probe, SMA905	GA-0042250	FDA UDI	Class II	Active
20GA Illuminating Laser Probe, SMA 906	GA-0040023	FDA UDI	Class II	Active
25GA Curved Illuminating Probe, SMA905	GA-0040077	FDA UDI	Class II	Active
20GA Straight Laser Probe, SMA906	GA-0040025	FDA UDI	Class II	Active
20GA Tapered Diffusion Light Pipe - 297 Connector	PD102.14	FDA UDI	Class II	Active
25GA Curved Laser Probe - Iridex	PD725.22	FDA UDI	Class II	Active
23GA Illuminating Laser Probe - Alcon	PD723.30	FDA UDI	Class II	Active
23GA Light Pipe - DORC	PD104.23	FDA UDI	Class II	Active
60 Degree DMEK/DSAEK Forceps	PD427.60	FDA UDI	Class I	Active
25GA Curved Illuminating Laser Probe - Iridex	PD725.37	FDA UDI	Class II	Active
25GA Curved Alcon Illuminating Laser Probe - Iridex - Short	PD725.37SA	FDA UDI	Class II	Active
20GA Light Pipe - Standard	PD103.00	FDA UDI	Class II	Active
20GA Straight Laser Probe, SMA905	GA-0040012	FDA UDI	Class II	Active
20GA Flexible 41GA Cannula	PD220.41	FDA UDI	Class I	Active
20GA Hard Tip Aspirating Laser Probe - Alcon	PD720.60HT	FDA UDI	Class II	Active
20GA Light Pipe - 297 Connector	PD102.00	FDA UDI	Class II	Active
20GA Curved Illuminating Probe, SMA905	GA-0042200	FDA UDI	Class II	Active
23GA Curved Alcon Illuminating Laser Probe - Iridex - PF	PD723.37A-PF	FDA UDI	Class II	Active
23GA Straight Laser Probe, SMA906	GA-0040022	FDA UDI	Class II	Active
20GA End Irrigating Light Pipe - 297 Connector	PD102.02	FDA UDI	Class II	Active
20GA Straight Laser Probe - HGM	PD720.11	FDA UDI	Class II	Active
27GA Curved Illuminating Laser Probe - DORC	7627.DORC-00	FDA UDI	Class II	Active
23GA Midfield Endoillumination Probe	3269.M06-00	FDA UDI	Class II	Active
20GA Alcon Illuminating Laser Probe - Alcon	PD720.30A	FDA UDI	Class II	Active
20GA Aspirating Laser Probe, SMA906	GA-0040013	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