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MICROSURGICAL TECHNOLOGY, INC.

United States·US-MF-000020475

Last updated September 17, 2026

Information

Country
United States
Address
8415 154TH AVE NE, REDMOND, United States
LinkedIn
—
Facebook
—
Phone
425-284-9409
PRRC Contact
Farha Shafi Ahmed
EUDAMED SRN
US-MF-000020475
FDA FEI Number
3019924
DUNS Number
—

Catalogue (881)

Page 17 of 18
DeviceModel / ReferenceRegistriesClassStatus
MST ICL Grasping Forceps DFH-0017
FDA UDI
Class IActive
MST/Dewey 0.9 Bent Mini A1 12° 30° PT-32030-P
FDA UDI
Class IIActive
MST Gold Silicone Sleeve SS-2207
FDA UDI
Class IActive
MST/Packard .7mm Straight Phaco Tip Dewey 30° PT-32430-B
FDA UDI
Class IIActive
MST/Dewey Mini Bent 45deg PT-30545-1
FDA UDI
Class IIActive
MST/Packard .7mm Straight P Tip 30° PT-32330-GRN
FDA UDI
Class IIActive
MST .7mm A1 Bent Phaco Tip 30° PT-31730-P
FDA UDI
Class IIActive
1X 23g Hfmn/Ahmd Hz Scissors, Cvd Shft DFH-1008-1
FDA UDI
Class IActive
MST Yellow Silicone Sleeve for 2.4-2.75 incision SIL-0001-Y
FDA UDI
Class IActive
20g Braga-Mele Irr Chopper, Ported Du-02319
FDA UDI
Class IActive
BRT V2 Bent, Cap Pl, 0.3 A1 0.7 Purple BRT-1029-P
FDA UDI
Class IActive
MST Light Blue Silicone Sleeve for 2.2-2.4 incision SIL-0003-B
FDA UDI
Class IActive
MST/Packard A1 .7mm Phaco Tip Bent Dewey 30° PT-33230-P
FDA UDI
Class IIActive
Swivel Guard Protector/Flush Tool DFA-0004
FDA UDI
Class IActive
MST/Dewey .9mm Ph Tip 15deg Bent PT-27415-1
FDA UDI
Class IIActive
MST A1 0.9mm Straight Tip Phaco Tip, 30º Bevel PT-33530
FDA UDI
Class IIActive
Curved Tip For Silicone Sleeve For InterTip™-T Titanium I/A System Ti-98309
FDA UDI
Class IActive
Medical Device Anterior Capsule Retractor MCR-0001
FDA UDI
Class IActive
MST/Packard .7mm straight PT Dwy 30° Single Use PT-32430-1
FDA UDI
Class IIActive
45° Tip For Silicone Sleeve For InterTip™-T Titanium I/A System Ti-98313
FDA UDI
Class IActive
MST/Packard A1 .7mm 12° Bent Phaco Tip, 45° PT-32245-1
FDA UDI
Class IIActive
19g Curved Aspiration .3mm Port Du-02341
FDA UDI
Class IActive
MST/Packard A1 .7mm 12° Bent Phaco Tip, 30° PT-32230-R
FDA UDI
Class IIActive
MST 0.9 Bent Mini A1 12° 45° PT-32145-P-1
FDA UDI
Class IIActive
MST/Packard .7mm Straight Phaco Tip 30° PT-32330-Y-1
FDA UDI
Class IIActive
BRT V2 Cvd, Cap Pl, 0.3, 0.7 gld BRT-1024
FDA UDI
Class IActive
Phaco Tip MST 0.9mm Str. A1 15deg PT-21915
FDA UDI
Class IIActive
BRT V2 Curved, Cap Pl, 0.3, 0.7 Blue BRT-1035-B
FDA UDI
Class IActive
BRT V2 Strt, Cap Pl, 0.3, 1.8inc bl BRT-1019
FDA UDI
Class IActive
MST Mini S2 Bent Phaco Tip 30deg PT-31930
FDA UDI
Class IIActive
Phaco Tip MST 1.1mm 30 Deg Bent PT-27730
FDA UDI
Class IIActive
BRT V2 Bnt, Cp Pl 0.3, A1 red BRT-1002
FDA UDI
Class IActive
MST/Dewey .09 Bent Mini A1 12°, 30° Bevel PT-32030-RNS
FDA UDI
Class IIActive
MST/Dewey .9mm A1 Bent Ph Tip 45de PT-22145
FDA UDI
Class IIActive
MST/Dewey Phaco Tip 0deg 20g PT-27300
FDA UDI
Class IIActive
I/A tip-2 flushkit (5 / bag) IH-90340
FDA UDI
Class IActive
MST/Packard A1 .7mm 12° Bent Phaco Tip, 45° PT-32245-G-1
FDA UDI
Class IIActive
MST .8mm Straight Phaco Tip 30 Deg PT-28130
FDA UDI
Class IIActive
MST/Dewey Phaco Tip 45deg 20g PT-27345
FDA UDI
Class IIActive
Malyugin Ring System 2.0, 6.25mm MAL-1001-1
FDA UDI
Class IActive
MST/Dewey 1.1mm Ph Tip 15deg Bent PT-28315-1
FDA UDI
Class IIActive
Phaco Tip MST 1.1mm A1 15deg, Bent PT-21715-1
FDA UDI
Class IIActive
MST/Packard A1 .7mm 12˚ Bend Phaco Tip, 45˚ PT-32245-R
FDA UDI
Class IIActive
MST Mini S2 Phaco Tip 45° PT-30845-1
FDA UDI
Class IIActive
MST/Packard A1 .7mm Phaco Tip, Reverse Bevel Bent PT-33330-G
FDA UDI
Class IIActive
MST/Packard A1 .7mm Phaco Tip Bent Dewey Reverse Bevel PT-33430-R-1
FDA UDI
Class IIActive
90° Tip For InterTip™-T Titanium I/A System Ti-98304
FDA UDI
Class IActive
45° Tip For Silicone Sleeve For InterTip™-T Titanium I/A Systemv TT-93313
FDA UDI
Class IActive
Phaco Tip MST 1.1mm A1 0deg, Bent PT-21700
FDA UDI
Class IIActive
Straight Tip, 0.5mm Port, Visco Removal For InterTip™-T Titanium I/A System TT-93321
FDA UDI
Class IActive

Related Companies

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Importers

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Notified Bodies

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Authorities

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FDA Recalls (2)

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
Aug 20, 2025Z-0411-2026—open, classified

An ophthalmic knife has a suction set (not direct patient-contacting), which contains springs contaminated with an unidentified residue that may potentially cause eye irritation

Sep 17, 2024Z-0521-2025—open, classified

Due to pin coming off of handles.