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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 3 of 35
DeviceModel / ReferenceRegistriesClassStatus
CoLink™ Afx P73 ST024
FDA UDI
Class IIActive
CoLink® 2 P42 ST235
FDA UDI
Class IIActive
Hercules A40 SP055
FDA UDI
Class IIActive
CoLink P04 N0103
FDA UDI
Class IIActive
CoLink P92 ST250
FDA UDI
Class IIActive
CoLink™ Afx P72 ST026
FDA UDI
Class IIActive
CoLink P92 ST011
FDA UDI
Class IIActive
CoLink P04 N0111
FDA UDI
Class IIActive
Ibs-B S40 ST852
FDA UDI
Class IIActive
5ms™ P64 ST713
FDA UDI
Class IIActive
CoLag 2 P67 ST245
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST760
FDA UDI
Class IIUnknown
CoLink™ Afx P74 ST038
FDA UDI
Class IIActive
Ibs-B S67 ST190
FDA UDI
Class IIActive
Ibs-B S40 ST750
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST750
FDA UDI
Class IIUnknown
CoLink P08 S0051
FDA UDI
Class IActive
CoLink® NeoFuse P20 ST123
FDA UDI
Class IIActive
CoLag 2 P67 ST252
FDA UDI
Class IIActive
Fracture and Correction CoLag™ P65 ST124
FDA UDI
Class IIUnknown
Ibs-B S67 ST255
FDA UDI
Class IIActive
CoLink™ Afx P73 ST055
FDA UDI
Class IIActive
CoLink C20 ST261
FDA UDI
Class IIActive
Hercules A20 SP245
FDA UDI
Class IIActive
CoLink Afx P07 N0151
FDA UDI
Class IActive
CoLag 2 P67 ST312
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST834
FDA UDI
Class IIUnknown
CoLink P04 N0171
FDA UDI
Class IIActive
CoLag™ P65 ST647
FDA UDI
Class IIActive
NeoSpan® T52 SN186
FDA UDI
Class IIUnknown
Ibs-B G01 N0082
FDA UDI
Class IActive
CoLink P92 ST208
FDA UDI
Class IIUnknown
Ibs-B S33 ST744
FDA UDI
Class IIActive
In2Bones P08 N0021
FDA UDI
Class IActive
CoLink P92 ST013
FDA UDI
Class IIActive
CoLink V50 ST024
FDA UDI
Class IIUnknown
CoLink™ Afx P73 ST045
FDA UDI
Class IIActive
Ibs-B S40 ST722
FDA UDI
Class IIActive
CoLink™ Afx P73 ST147
FDA UDI
Class IIActive
CoLink P08 N1203
FDA UDI
Class IActive
CoLag™ P65 ST440
FDA UDI
Class IIUnknown
CoLink® Mfx C20 ST111
FDA UDI
Class IIActive
5ms™ P60 ST780
FDA UDI
Class IIActive
CoLink™ View P40 ST241
FDA UDI
Class IIActive
CoLag 2 P68 ST160
FDA UDI
Class IIActive
CoLag™ P65 ST430
FDA UDI
Class IIUnknown
Fracture and Correction CoLag™ 2 P67 ST847
FDA UDI
Class IIActive
CoLink™ Afx P73 ST057
FDA UDI
Class IIActive
CoLink® P43 ST045
FDA UDI
Class IIActive
Quantum M05 00971
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.