FDA.reportPublic FDA data

AXIA ORTHOPEDICS

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30429531903042953190AXIA ORTHOPEDICS1N2026-01-012505 Se 11th Ave Ste 245 Portland OR US 97202

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00850083430009SOLOFIX Provisional Fixation System - 1.6MM (.062”) WIRE LOCK503-217-4226customerservice@axiaortho.com
00850083430061SOLOFIX Provisional Fixation System - 50MM EXTENDER503-217-4226customerservice@axiaortho.com
00850083430078SOLOFIX Provisional Fixation System - 1.6MM (.062”) COMPRESSION HANDLE503-217-4226customerservice@axiaortho.com
00850083430092SOLOFIX Provisional Fixation System - 2.4MM (.094”) COMPRESSION HANDLE503-217-4226customerservice@axiaortho.com
00850083430108SOLOFIX Provisional Fixation System - 1.6MM (.062”) K-WIRE WITH 10MM THREADED-TROCAR POINT, 229MM (9”)503-217-4226customerservice@axiaortho.com
00850083430122SOLOFIX Provisional Fixation System - 2.4MM (.094”) K-WIRE WITH 15MM THREADED-TROCAR POINT, 229MM (9”)503-217-4226customerservice@axiaortho.com
00850083430139SOLOFIX Provisional Fixation System - 2.4MM (.094”) PARTIALLY THREADED DRILL 229MM (9”)503-217-4226customerservice@axiaortho.com

Registered Device Listings#

Registration key, Listing key table
Registration keyListing key
3461371912921569
3461371984726986
3461372003419054

GUDID#