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In2Bones, USA

United States·US-MF-000023092

Last updated September 17, 2026

Information

Country
United States
Address
7750a, Trinity Road, Cordova, United States
LinkedIn
—
Facebook
—
Phone
+18664266633
PRRC Contact
Brent Lalomia
EUDAMED SRN
US-MF-000023092
FDA FEI Number
3011580264
DUNS Number
—

Catalogue (1746)

Page 11 of 35
DeviceModel / ReferenceRegistriesClassStatus
CoLink® NeoFuse V45 ST650
FDA UDI
Class IIUnknown
CoLink® P43 ST120
FDA UDI
Class IIActive
CoLag 2 P67 ST109
FDA UDI
Class IIActive
CoLink™ View P40 ST614
FDA UDI
Class IIActive
Avenger M70 SC355
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST728
FDA UDI
Class IIUnknown
Ibs-B S33 ST732
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST618
FDA UDI
Class IIUnknown
Ibs-B S40 ST728
FDA UDI
Class IIActive
CoLink Mini P90 ST105
FDA UDI
Class IIActive
In2Bones P04 S0232
FDA UDI
Class IActive
CoLink® NeoFuse V45 ST660
FDA UDI
Class IIUnknown
CoLink P92 ST230
FDA UDI
Class IIActive
In2Bones C01 N0015
FDA UDI
Class IActive
CoLag™ P65 ST428
FDA UDI
Class IIUnknown
CoLag 2 P67 ST142
FDA UDI
Class IIActive
Fracture and Correction CoLag™ P65 ST113
FDA UDI
Class IIUnknown
CoLink C20 ST281
FDA UDI
Class IIActive
Ibs-B S40 ST836
FDA UDI
Class IIActive
Ibs-B S67 ST305
FDA UDI
Class IIActive
CoLink P04 N0431
FDA UDI
Class IActive
CoLink™ View P40 ST161
FDA UDI
Class IIActive
CoLink P04 N0131
FDA UDI
Class IIActive
CoLink® 2 P42 ST012
FDA UDI
Class IIActive
CoLink Cfx P08 N0062
FDA UDI
Class IActive
CoLink® Mfx C20 ST231
FDA UDI
Class IIActive
5ms™ P60 ST547
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST828
FDA UDI
Class IIUnknown
CoLink® P43 ST020
FDA UDI
Class IIActive
CoLink™ Afx P73 ST036
FDA UDI
Class IIActive
In2Bones C01 N0168
FDA UDI
Class IActive
CoLink™ V35 ST424
FDA UDI
Class IIUnknown
5ms™ P64 ST409
FDA UDI
Class IIActive
CoLink® P40 ST135
FDA UDI
Class IIActive
CoLink Cfx P08 N0061
FDA UDI
Class IActive
CoLag 2 P67 ST426
FDA UDI
Class IIActive
Fracture and Correction CoLag™ 2 P67 ST690
FDA UDI
Class IIActive
CoLink™ Afx P72 ST037
FDA UDI
Class IIActive
NeoSpan T50 SN110
FDA UDI
Class IIUnknown
Ibs-B S33 ST850
FDA UDI
Class IIActive
CoLink Mini P90 ST016
FDA UDI
Class IIActive
CoLink P92 ST145
FDA UDI
Class IIActive
CoLink™ Afx P73 ST228
FDA UDI
Class IIActive
Fracture and Correction CoLag™ 2 P67 ST650
FDA UDI
Class IIActive
CoLink P70 ST301
FDA UDI
Class IIActive
Ibs-B S67 ST195
FDA UDI
Class IIActive
5ms™ P62 ST424
FDA UDI
Class IIActive
CoLink P92 ST035
FDA UDI
Class IIActive
Hercules A02 S0005
FDA UDI
Class IActive
5ms™ P60 ST011
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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 18, 2021Z-2506-2021—terminated

Complaints were received of CoLink Bone Graft Harvesters breaking at the outer tube weld site.

Nov 14, 2018Z-0670-2019—terminated

The NeoSpan Compression Staple (10x10x10) kits from two lots contain the wrong size drill bit. They contain a 3mm drill bit instead of a 2mm drill bit.