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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 16 of 35
DeviceModel / ReferenceRegistriesClassStatus
Ibs-B S33 ST738
FDA UDI
Class IIActive
CoLag™ P65 ST910
FDA UDI
Class IIActive
CoLink® P43 ST024
FDA UDI
Class IIActive
In2Bones C01 NCD50
FDA UDI
Class IActive
SubChon C01 S1207
FDA UDI
Class IActive
CoLink Mini P09 N1107
FDA UDI
Class IActive
Ibs-B S33 ST716
FDA UDI
Class IIActive
CoLink™ Afx P74 ST052
FDA UDI
Class IIActive
CoLag 2 P67 ST150
FDA UDI
Class IIActive
CoLink® 2 P42 ST135
FDA UDI
Class IIActive
In2Bones P06 S2731
FDA UDI
Class IActive
CoLink P92 ST228
FDA UDI
Class IIActive
CoLink P08 N1113
FDA UDI
Class IActive
Ibs-B S40 ST826
FDA UDI
Class IIActive
CoLag™ P65 ST630
FDA UDI
Class IIActive
CoLink™ Afx P72 ST247
FDA UDI
Class IIUnknown
In2Bones C01 N0072
FDA UDI
Class IActive
5ms™ P64 ST724
FDA UDI
Class IIActive
Ibs-B S40 ST850
FDA UDI
Class IIActive
5ms™ P62 ST415
FDA UDI
Class IIActive
Ibs-B S40 ST738
FDA UDI
Class IIActive
CoLink™ Afx P72 ST132
FDA UDI
Class IIActive
CoLink Mini P90 ST207
FDA UDI
Class IIActive
Avenger M70 SC155
FDA UDI
Class IIActive
CoLag 2 P67 ST326
FDA UDI
Class IIActive
CoLag™ P65 ST645
FDA UDI
Class IIActive
NeoSpan® T52 SN302
FDA UDI
Class IIUnknown
5ms P06 N0001
FDA UDI
Class IActive
SubChon C01 S1007
FDA UDI
Class IActive
5ms™ P60 ST765
FDA UDI
Class IIActive
5ms™ P64 ST710
FDA UDI
Class IIActive
CoLink P92 ST211
FDA UDI
Class IIActive
Avenger M70 SC395
FDA UDI
Class IIActive
5ms P06 N1021
FDA UDI
Class IIActive
In2Bones G01 S0082
FDA UDI
Class IActive
Ibs-B S67 ST230
FDA UDI
Class IIActive
CoLag 2 P67 ST115
FDA UDI
Class IIActive
CoLink™ Afx P73 ST130
FDA UDI
Class IIActive
Fracture and Correction CoLag™ 2 P67 ST877
FDA UDI
Class IIActive
CoLink™ Afx P73 ST155
FDA UDI
Class IIActive
CoLink™ Afx P73 ST150
FDA UDI
Class IIActive
Fracture and Correction CoLag™ 2 P67 ST910
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST616
FDA UDI
Class IIUnknown
CoLink™ Afx P73 ST038
FDA UDI
Class IIActive
CoLag™ P65 ST640
FDA UDI
Class IIActive
AlloAid C01 S0003
FDA UDI
Class IActive
Ibs-B S33 ST742
FDA UDI
Class IIActive
CoLink™ V35 ST438
FDA UDI
Class IIUnknown
Ibs-B S33 ST828
FDA UDI
Class IIActive
CoLink® 2 P42 ST145
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.