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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 12 of 35
DeviceModel / ReferenceRegistriesClassStatus
5ms™ P60 ST465
FDA UDI
Class IIActive
Ibs-B S67 ST150
FDA UDI
Class IIActive
CoLink® NeoFuse P20 ST233
FDA UDI
Class IIActive
CoLag™ P65 ST434
FDA UDI
Class IIUnknown
In2Bones C01 N0012
FDA UDI
Class IActive
CoLink V50 ST034
FDA UDI
Class IIUnknown
CoLink Mini P90 ST025
FDA UDI
Class IIActive
Ibs-B S33 ST818
FDA UDI
Class IIActive
CoLag 2 P67 ST216
FDA UDI
Class IIActive
Ibs-B S67 ST615
FDA UDI
Class IIActive
5ms™ P60 ST645
FDA UDI
Class IIActive
CoLink™ View P40 ST136
FDA UDI
Class IIActive
CoLag™ P65 ST662
FDA UDI
Class IIActive
In2Bones C01 N0111
FDA UDI
Class IActive
CoLink® 2 P43 ST226
FDA UDI
Class IIUnknown
Fracture and Correction CoLag™ 2 P67 ST915
FDA UDI
Class IIActive
CoLink P92 ST009
FDA UDI
Class IIActive
Ibs-B S40 ST752
FDA UDI
Class IIActive
Avenger M70 HC020
FDA UDI
Class IIActive
Ibs-B S40 ST726
FDA UDI
Class IIActive
Fracture and Correction CoLag™ 2 P68 ST267
FDA UDI
Class IIActive
Fracture and Correction CoLag™ 2 P67 ST670
FDA UDI
Class IIActive
CoLink Mfx C02 N1502
FDA UDI
Class IActive
CoLink Mini P09 N0041
FDA UDI
Class IActive
CoLink® P43 ST052
FDA UDI
Class IIActive
CoLink™ Afx P72 ST050
FDA UDI
Class IIActive
In2Bones P06 N0551
FDA UDI
Class IActive
In2Bones C01 N1012
FDA UDI
Class IActive
CoLink® 2 P42 ST023
FDA UDI
Class IIActive
CoLink® 2 P43 ST230
FDA UDI
Class IIUnknown
CoLink Afx P07 N0231
FDA UDI
Class IActive
CoLink P04 N0122
FDA UDI
Class IIActive
CoLag 2 P67 ST250
FDA UDI
Class IIActive
CoLink G05 S1008
FDA UDI
Class IActive
CoLink® P43 ST132
FDA UDI
Class IIActive
NeoSpan T50 SN018
FDA UDI
Class IIUnknown
5ms™ P60 ST665
FDA UDI
Class IIActive
CoLink™ Afx P70 ST107
FDA UDI
Class IIActive
NeoSpan® T52 SN181
FDA UDI
Class IIUnknown
CoLink® P43 ST040
FDA UDI
Class IIActive
Ibs-B S40 ST854
FDA UDI
Class IIActive
CoLink Cfx P80 ST212
FDA UDI
Class IIActive
5ms™ P60 ST555
FDA UDI
Class IIActive
In2Bones C01 N0081
FDA UDI
Class IActive
CoLink Mini P90 ST205
FDA UDI
Class IIActive
CoLag™ P65 ST224
FDA UDI
Class IIUnknown
CoLink V50 ST030
FDA UDI
Class IIUnknown
5ms™ P60 ST640
FDA UDI
Class IIActive
CoLink™ Afx P72 ST024
FDA UDI
Class IIActive
CoLag 2 P67 ST224
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.