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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 29 of 35
DeviceModel / ReferenceRegistriesClassStatus
CoLink Mfx C02 N1301
FDA UDI
Class IActive
CoLink P92 ST224
FDA UDI
Class IIActive
CoLink Vallux P90 ST031
FDA UDI
Class IIActive
In2Bones P07 N0021
FDA UDI
Class IActive
In2Bones P06 N0452
FDA UDI
Class IActive
Hercules A20 SP220
FDA UDI
Class IIActive
CoLink P92 ST022
FDA UDI
Class IIActive
NeoSpan® T52 SN118
FDA UDI
Class IIUnknown
Ibs-B S40 ST746
FDA UDI
Class IIActive
CoLag 2 P67 ST430
FDA UDI
Class IIActive
CoLink P08 N1101
FDA UDI
Class IActive
CoLag™ P65 ST336
FDA UDI
Class IIUnknown
CoLink® NeoFuse V45 ST732
FDA UDI
Class IIUnknown
Ibs-B S67 ST570
FDA UDI
Class IIActive
CoLink® P40 SP012
FDA UDI
Class IIActive
CoLink Cfx P80 ST111
FDA UDI
Class IIActive
CoLink® P43 ST032
FDA UDI
Class IIActive
CoLink™ Afx P70 ST209
FDA UDI
Class IIActive
CoLink Cfx P08 N0081
FDA UDI
Class IActive
CoLink P92 ST026
FDA UDI
Class IIActive
CoLink P04 N0242
FDA UDI
Class IActive
NeoSpan T50 SN120
FDA UDI
Class IIUnknown
In2Bones C01 N0009
FDA UDI
Class IActive
CoLink P92 ST012
FDA UDI
Class IIActive
CoLag™ P65 ST565
FDA UDI
Class IIActive
CoLink® 2 P43 ST218
FDA UDI
Class IIUnknown
5ms™ P62 ST709
FDA UDI
Class IIActive
Avenger M70 SC185
FDA UDI
Class IIActive
CoLink™ Afx P72 ST150
FDA UDI
Class IIActive
CoLink Afx P07 N1106
FDA UDI
Class IIActive
Hercules A04 S0025
FDA UDI
Class IActive
CoLink™ Afx P72 ST142
FDA UDI
Class IIUnknown
CoLink™ Afx P73 ST255
FDA UDI
Class IIActive
Ibs-B S33 ST720
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST624
FDA UDI
Class IIUnknown
CoLink P92 ST110
FDA UDI
Class IIActive
CoLink™ Afx P74 ST028
FDA UDI
Class IIActive
5ms™ P60 ST770
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST636
FDA UDI
Class IIUnknown
CoLink® 2 P43 ST232
FDA UDI
Class IIUnknown
CoLink Cfx P80 ST241
FDA UDI
Class IIActive
Fracture and Correction CoLag™ 2 P67 ST887
FDA UDI
Class IIActive
CoLink™ Afx P73 ST138
FDA UDI
Class IIActive
CoLag 2 P68 ST155
FDA UDI
Class IIActive
CoLink Afx P07 N0111
FDA UDI
Class IActive
CoLink™ Afx P70 ST103
FDA UDI
Class IIActive
CoLink™ View P40 SP631
FDA UDI
Class IIActive
CoLink™ Afx P74 ST010
FDA UDI
Class IIActive
NeoSpan® T52 SN300
FDA UDI
Class IIUnknown
CoLink™ Afx P73 ST126
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.