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Orthalign, Inc.

United States·US-MF-000027362

Last updated September 17, 2026

Information

Country
United States
Address
153, Technology, Irvine, United States
LinkedIn
—
Facebook
—
Phone
949.715.2424
PRRC Contact
Karyl Haskell
EUDAMED SRN
US-MF-000027362
FDA FEI Number
3007521480
DUNS Number
023266163

Catalogue (373)

Page 5 of 8
DeviceModel / ReferenceRegistriesClassStatus
Lantern Surgical Assistant 402532-02
FDA UDI
Class IIActive
KneeAlign 2 402066-1
FDA UDI
Class IIActive
OrthAlign Plus 403484
FDA UDI
Class IIActive
Lantern Surgical Assistant (LSA) 402472
FDA UDI
Class IIActive
KneeAlign 2 402066-3
FDA UDI
Class IIActive
OrthAlign Plus 403414
FDA UDI
Class IIActive
Lantern Surgical Assistant (LSA) 402505
FDA UDI
Class IIActive
OrthAlign Plus 403247
FDA UDI
Class IIActive
OrthAlign Plus 403007-08
FDA UDI
Class IIActive
OrthAlign Plus 403001-07-CE
FDA UDI
Class IIActive
OrthAlign Plus 403218-03
FDA UDI
Class IIActive
OrthAlign Plus 402145
FDA UDI
Class IIActive
OrthAlign Plus 403007-20
FDA UDI
Class IIActive
OrthAlign Plus 402073-2
FDA UDI
Class IIActive
Lantern Surgical Assistant 402528-04
FDA UDI
Class IIActive
OrthAlign Plus 401745
FDA UDI
Class IIActive
Lantern 502000-01
FDA UDI
Class IIActive
OrthAlign Plus 403373
FDA UDI
Class IIActive
KneeAlign 2 401483
FDA UDI
Class IIActive
OrthAlign Plus 402148
FDA UDI
Class IIActive
OrthAlign Plus 401638
FDA UDI
Class IIActive
OrthAlign Plus 403169
FDA UDI
Class IIActive
Lantern Surgical Assistant 402519-04
FDA UDI
Class IIActive
KneeAlign 2 402066-5
FDA UDI
Class IIActive
OrthAlign Plus 402147
FDA UDI
Class IIActive
OrthAlign Plus 403423
FDA UDI
Class IIActive
OrthAlign Plus 403007-02
FDA UDI
Class IIActive
OrthAlign Plus 403187
FDA UDI
Class IIActive
KneeAlign 2 401575
FDA UDI
Class IIActive
Lantern 403566
FDA UDI
Class IIActive
KneeAlign 2 402064-07
FDA UDI
Class IIActive
Harvey Surgical Assistant (HSA) 402127
FDA UDI
Class IIActive
OrthAlign Plus 402128
FDA UDI
Class IIActive
OrthAlign Plus 403188
FDA UDI
Class IIActive
Lantern Surgical Assistant 402519-03
FDA UDI
Class IIActive
KneeAlign 2 402097
FDA UDI
Class IIActive
Lantern Surgical Assistant (LSA) 405204-KA
FDA UDI
Class IIActive
Lantern Surgical Assistant (LSA) 402475
FDA UDI
Class IIActive
Lantern 403569
FDA UDI
Class IIActive
OrthAlign Plus 403284
FDA UDI
Class IIActive
OrthAlign Plus 403480
FDA UDI
Class IIActive
OrthAlign Plus 403415
FDA UDI
Class IIActive
OrthAlign Plus 403211
FDA UDI
Class IIActive
KneeAlign 401629
FDA UDI
Class IActive
OrthAlign Plus 403218-02
FDA UDI
Class IIActive
OrthAlign Plus 403341
FDA UDI
Class IIActive
OrthAlign Plus 402105
FDA UDI
Class IIActive
KneeAlign 2 402047-03
FDA UDI
Class IIActive
KneeAlign 2 402066-4
FDA UDI
Class IIActive
OrthAlign Plus 403324
FDA UDI
Class IIActive

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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
Feb 10, 2026Z-1630-2026—open, classified

Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)

Feb 10, 2026Z-1629-2026—open, classified

Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)