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MIRA, INC.

Last updated September 17, 2026

Information

Country: US
Address: 414 Quaker Hwy, UXBRIDGE, MA, 01569
Website: mirainc.us
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: 5082787877
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 1218813
DUNS Number: 001414358

Catalogue (81)

Page 1 of 2

Device	Model / Reference	Registries	Class	Status
MIRA IMEX Scleral Buckling Component	286	FDA UDI	Class II	Active
MIRA Cryosurgical Probe, Gaynon Curved Cataract	CR4085	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	225	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	270	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	505G	FDA UDI	Class II	Active
MIRA Cryosurgical Probe, Straight Vitreous	CR4040	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	42	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	508G	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	517	FDA UDI	Class II	Active
MIRA Cryosurgical Probe, Curved Cataract	CR4023	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	75R	FDA UDI	Class II	Active
MIRA Cryosurgical Probe, Abramson Retinoblastoma	CR4090	FDA UDI	Class II	Active
MIRA Cryosurgical Probe, Curved Glaucoma	CR4030	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	276	FDA UDI	Class II	Active
MIRA Cryosurgical Probe, Lashkari Trichiasis	CR4095	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	502	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	507	FDA UDI	Class II	Active
MIRA Cryosurgical Probe, Hammerhead	CR4075	FDA UDI	Class II	Active
MIRA Cryosurgical Console	CR4000	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	505	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	219	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	503	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	507T	FDA UDI	Class II	Active
MIRA Cryosurgical Probe, Baby Hammerhead	CR4080	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	509G	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	505T	FDA UDI	Class II	Active
MIRA Cryosurgical Probe, Straight Mini Vitreous	CR4045	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	509	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	507G	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	504	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	5	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	72	FDA UDI	Class II	Active
MIRA Cryosurgical Probe, Straight Cataract	CR4022	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	508	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	40	FDA UDI	Class II	Active
MIRA Cryosurgical Probe, Mini Curved Cataract	CR4025	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	220	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	501	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	277	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	41	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	287	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	506	FDA UDI	Class II	Active
MIRA Cryosurgical Probe, Curved Retinal	CR4010	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	516G	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	250	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	506G	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	106	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	32	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	5025	FDA UDI	Class II	Active
MIRA IMEX Scleral Buckling Component	240	FDA UDI	Class II	Active

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FDA Recalls (3)

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
Apr 8, 2010	Z-1919-2010	—	terminated	Devices distributed without an approved 510(k)
Apr 8, 2010	Z-1920-2010	—	terminated	Devices distributed without an approved 510(k)
Apr 8, 2010	Z-1918-2010	—	terminated	Devices distributed without an approved 510(k)