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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 26 of 35
DeviceModel / ReferenceRegistriesClassStatus
CoLink® P43 ST118
FDA UDI
Class IIActive
CoLink® P43 ST160
FDA UDI
Class IIActive
Fracture and Correction CoLag™ P65 ST130
FDA UDI
Class IIUnknown
CoLink Afx P07 N1401
FDA UDI
Class IIActive
Fracture and Correction CoLag™ 2 P67 ST905
FDA UDI
Class IIActive
Ibs-B S33 ST858
FDA UDI
Class IIActive
CoLink™ Afx P72 ST232
FDA UDI
Class IIActive
CoLink® P43 ST022
FDA UDI
Class IIActive
CoLink™ Afx P74 ST040
FDA UDI
Class IIActive
CoLink P04 N0212
FDA UDI
Class IIActive
5ms™ P64 ST728
FDA UDI
Class IIActive
Ibs-B S33 ST724
FDA UDI
Class IIActive
CoLink® P43 ST147
FDA UDI
Class IIActive
SubChon C01 S1009
FDA UDI
Class IActive
Ibs-B S67 ST160
FDA UDI
Class IIActive
Avenger M70 SC075
FDA UDI
Class IIActive
In2Bones P07 N0191
FDA UDI
Class IActive
CoLink™ Afx P73 ST110
FDA UDI
Class IIActive
Avenger M70 HC022
FDA UDI
Class IIActive
CoLag™ P65 ST677
FDA UDI
Class IIActive
CoLag 2 P67 ST328
FDA UDI
Class IIActive
In2Bones C01 S2268
FDA UDI
Class IActive
5ms™ P64 ST726
FDA UDI
Class IIActive
Ibs-B S40 ST820
FDA UDI
Class IIActive
CoLink™ Afx P70 ST006
FDA UDI
Class IIActive
CoLag™ P65 ST552
FDA UDI
Class IIActive
In2Bones P09 N0031
FDA UDI
Class IActive
Ibs-B S33 ST728
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST724
FDA UDI
Class IIUnknown
CoLink® NeoFuse V45 ST745
FDA UDI
Class IIUnknown
SubChon C01 S1505
FDA UDI
Class IActive
CoLag P06 N0003
FDA UDI
Class IActive
Ibs-B S40 ST838
FDA UDI
Class IIActive
Avenger M70 HC218
FDA UDI
Class IIActive
CoLink™ Afx P72 ST245
FDA UDI
Class IIActive
CoLag™ P65 ST836
FDA UDI
Class IIActive
Ibs-B S40 ST858
FDA UDI
Class IIActive
CoLink™ Afx P73 ST112
FDA UDI
Class IIActive
In2Bones C01 N0023
FDA UDI
Class IActive
5ms™ P60 ST750
FDA UDI
Class IIActive
In2Bones P04 S0003
FDA UDI
Class IActive
Fracture and Correction CoLag™ 2 P67 ST857
FDA UDI
Class IIActive
CoLink® Sfx K24 SS311
FDA UDI
Class IIActive
In2Bones P02 N0111
FDA UDI
Class IActive
CoLink P92 ST122
FDA UDI
Class IIActive
CoLag™ P65 ST452
FDA UDI
Class IIUnknown
Avenger M07 N0024
FDA UDI
Class IActive
Fracture and Correction CoLag™ P65 ST115
FDA UDI
Class IIUnknown
CoLink® P43 ST110
FDA UDI
Class IIActive
CoLink P08 N1112
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.