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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 9 of 35
DeviceModel / ReferenceRegistriesClassStatus
CoLink® Sfx K24 SS211
FDA UDI
Class IIActive
CoLink™ Afx P73 ST242
FDA UDI
Class IIActive
CoLink™ View P40 ST261
FDA UDI
Class IIActive
5ms™ P60 ST447
FDA UDI
Class IIActive
In2Bones P08 N0011
FDA UDI
Class IActive
Avenger M07 S0003
FDA UDI
Class IActive
CoLink® NeoFuse V45 ST718
FDA UDI
Class IIUnknown
Ibs-B G01 N0112
FDA UDI
Class IActive
CoLag 2 P67 ST318
FDA UDI
Class IIActive
CoLag™ P65 ST460
FDA UDI
Class IIUnknown
CoLag™ P65 ST422
FDA UDI
Class IIUnknown
CoLink™ View P40 ST236
FDA UDI
Class IIActive
CoLag 2 P67 ST457
FDA UDI
Class IIActive
Fracture and Correction CoLag™ 2 P67 ST882
FDA UDI
Class IIActive
In2Bones P08 N0051
FDA UDI
Class IActive
CoLink P08 N1202
FDA UDI
Class IActive
AlloAid C01 SCM01
FDA UDI
Class IActive
5ms™ P64 ST410
FDA UDI
Class IIActive
CoLag™ P65 ST312
FDA UDI
Class IIUnknown
CoLink™ V35 ST432
FDA UDI
Class IIUnknown
Avenger M70 HC024
FDA UDI
Class IIActive
5ms™ P64 ST426
FDA UDI
Class IIActive
CoLink® P43 ST128
FDA UDI
Class IIActive
CoLink® P43 ST016
FDA UDI
Class IIActive
Ibs-B S33 ST848
FDA UDI
Class IIActive
Ibs-B S33 ST756
FDA UDI
Class IIActive
5ms P06 N0041
FDA UDI
Class IActive
In2Bones C01 N0017
FDA UDI
Class IActive
Ibs-B S33 ST822
FDA UDI
Class IIActive
Ibs-B S33 ST844
FDA UDI
Class IIActive
CoLink™ Afx P73 ST116
FDA UDI
Class IIActive
CoLag™ P65 ST530
FDA UDI
Class IIActive
CoLink™ Afx P72 ST222
FDA UDI
Class IIActive
CoLink™ Afx P74 ST036
FDA UDI
Class IIActive
CoLink® P40 ST012
FDA UDI
Class IIActive
Fracture and Correction CoLag™ 2 P67 ST885
FDA UDI
Class IIActive
5ms™ P60 ST043
FDA UDI
Class IIActive
CoLag™ P65 ST220
FDA UDI
Class IIUnknown
5ms™ P60 ST455
FDA UDI
Class IIActive
CoLink P04 N0132
FDA UDI
Class IIActive
CoLag 2 P67 ST222
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST830
FDA UDI
Class IIUnknown
CoLink™ Afx P73 ST210
FDA UDI
Class IIActive
Fracture and Correction CoLag™ 2 P67 ST675
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST820
FDA UDI
Class IIUnknown
Rts M30 SE030
FDA UDI
Class IIActive
CoLink V50 ST036
FDA UDI
Class IIUnknown
Avenger M07 N0022
FDA UDI
Class IActive
CoLag™ P65 ST905
FDA UDI
Class IIActive
In2Bones C01 N1031
FDA UDI
Class IActive

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.