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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 20 of 35
DeviceModel / ReferenceRegistriesClassStatus
Fracture and Correction CoLag™2 P67 ST536
FDA UDI
Class IIActive
Ibs-B S33 ST758
FDA UDI
Class IIActive
CoLink V50 ST060
FDA UDI
Class IIUnknown
5ms™ P62 ST412
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST838
FDA UDI
Class IIUnknown
Fracture and Correction CoLag™ P65 ST108
FDA UDI
Class IIUnknown
CoLink® 2 P42 ST055
FDA UDI
Class IIActive
CoLink™ Afx P73 ST022
FDA UDI
Class IIActive
CoLink™ Afx P72 ST108
FDA UDI
Class IIActive
CoLink® Sfx K24 SS114
FDA UDI
Class IIActive
CoLink® 2 P43 ST242
FDA UDI
Class IIUnknown
In2Bones P06 N0711
FDA UDI
Class IActive
5ms™ P64 ST711
FDA UDI
Class IIActive
5ms™ P60 ST031
FDA UDI
Class IIActive
CoLag 2 P67 ST120
FDA UDI
Class IIActive
CoLink™ Afx P72 ST214
FDA UDI
Class IIActive
Fracture and Correction CoLag™ 2 P67 ST655
FDA UDI
Class IIActive
Ibs-B S67 ST270
FDA UDI
Class IIActive
CoLink P92 ST032
FDA UDI
Class IIActive
CoLink P92 ST212
FDA UDI
Class IIActive
CoLink® Sfx K24 SS111
FDA UDI
Class IIActive
CoLink™ View P40 SP621
FDA UDI
Class IIActive
CoLag™ P65 ST872
FDA UDI
Class IIActive
CoLag™ P65 ST438
FDA UDI
Class IIUnknown
5ms™ P60 ST033
FDA UDI
Class IIActive
CoLink Mfx C02 N1101
FDA UDI
Class IActive
CoLink® NeoFuse V45 ST840
FDA UDI
Class IIUnknown
CoLink™ V35 ST428
FDA UDI
Class IIUnknown
Fracture and Correction CoLag™ 2 P68 ST255
FDA UDI
Class IIActive
CoLink P92 ST015
FDA UDI
Class IIActive
CoLink V50 ST028
FDA UDI
Class IIUnknown
Ibs-B S40 ST744
FDA UDI
Class IIActive
CoLag 2 P67 ST145
FDA UDI
Class IIActive
CoLag 2 P67 ST332
FDA UDI
Class IIActive
CoLink P92 ST037
FDA UDI
Class IIActive
In2Bones P07 N0211
FDA UDI
Class IActive
5ms™ P60 ST752
FDA UDI
Class IIActive
5ms P06 N1022
FDA UDI
Class IIActive
Avenger M07 S0001
FDA UDI
Class IActive
CoLink® 2 P42 ST239
FDA UDI
Class IIActive
CoLink™ Afx P72 ST228
FDA UDI
Class IIActive
Hercules A02 S0004
FDA UDI
Class IActive
5ms™ P64 ST420
FDA UDI
Class IIActive
5ms™ P60 ST440
FDA UDI
Class IIActive
5ms™ P62 ST726
FDA UDI
Class IIActive
CoLag™ P65 ST860
FDA UDI
Class IIActive
CoLink® 2 P43 ST257
FDA UDI
Class IIUnknown
5ms™ P60 ST560
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST855
FDA UDI
Class IIUnknown
CoLink™ Afx P73 ST236
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.