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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 17 of 35
DeviceModel / ReferenceRegistriesClassStatus
5ms™ P62 ST409
FDA UDI
Class IIActive
CoLink® P43 ST034
FDA UDI
Class IIActive
CoLink Afx P07 N0241
FDA UDI
Class IActive
In2Bones C01 N0002
FDA UDI
Class IActive
CoLink P92 ST018
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST640
FDA UDI
Class IIUnknown
CoLink™ Afx P73 ST032
FDA UDI
Class IIActive
Ibs-B S67 ST250
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST622
FDA UDI
Class IIUnknown
CoLag 2 P67 ST132
FDA UDI
Class IIActive
CoLag™ P65 ST915
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST680
FDA UDI
Class IIUnknown
CoLink Mfx C02 N0021
FDA UDI
Class IActive
CoLink® NeoFuse V45 ST740
FDA UDI
Class IIUnknown
Fracture and Correction CoLag™ P65 ST114
FDA UDI
Class IIUnknown
5ms™ P64 ST411
FDA UDI
Class IIActive
CoLink® 2 P42 ST237
FDA UDI
Class IIActive
CoLink P92 ST222
FDA UDI
Class IIActive
Fracture and Correction CoLag™ 2 P67 ST632
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST620
FDA UDI
Class IIUnknown
5ms™ P64 ST716
FDA UDI
Class IIActive
CoLink™ Afx P72 ST030
FDA UDI
Class IIActive
5ms™ P62 ST718
FDA UDI
Class IIActive
In2Bones P06 S2721
FDA UDI
Class IActive
CoLink® NeoFuse V45 ST824
FDA UDI
Class IIUnknown
CoLink® Sfx K24 SS154
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST632
FDA UDI
Class IIUnknown
Ibs-B S33 ST750
FDA UDI
Class IIActive
In2Bones C01 N0019
FDA UDI
Class IActive
Hercules A04 S0045
FDA UDI
Class IActive
CoLink™ Afx P72 ST147
FDA UDI
Class IIUnknown
5ms™ P62 ST712
FDA UDI
Class IIActive
Ibs-B S40 ST734
FDA UDI
Class IIActive
In2Bones P07 N0181
FDA UDI
Class IActive
5ms P06 N0031
FDA UDI
Class IActive
CoLink™ Afx P72 ST242
FDA UDI
Class IIUnknown
CoLink P04 N0221
FDA UDI
Class IActive
CoLag™ P65 ST852
FDA UDI
Class IIActive
CoLink Mfx C02 N0051
FDA UDI
Class IActive
Ibs-B S40 ST732
FDA UDI
Class IIActive
CoLink™ Afx P73 ST028
FDA UDI
Class IIActive
CoLag 2 P67 ST322
FDA UDI
Class IIActive
5ms™ P64 ST709
FDA UDI
Class IIActive
CoLink™ V30 ST232
FDA UDI
Class IIUnknown
CoLink P92 ST140
FDA UDI
Class IIActive
CoLink® NeoFuse P20 ST133
FDA UDI
Class IIActive
5ms™ P64 ST414
FDA UDI
Class IIActive
SubChon M08 N0011
FDA UDI
Class IActive
5ms™ P64 ST715
FDA UDI
Class IIActive
5ms™ P64 ST722
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.