← Back to manufacturers

Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

TOTAL JOINT ORTHOPEDICS, INC.

US

Last updated September 17, 2026

Information

Country
US
Address
1567 E. Stratford Avenue, Salt Lake City, UT, 84106
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
3008544874
DUNS Number
—

Catalogue (2063)

Page 36 of 42
DeviceModel / ReferenceRegistriesClassStatus
Stem Trial 2015.12.040
FDA UDI
Class IActive
Stem Trial 2015.10.100
FDA UDI
Class IActive
Klassic BiPolar Trial 1322.39.022
FDA UDI
Class IActive
Modular Femoral Head Trial 1326.32.000
FDA UDI
Class IActive
Acetabular Insert Impactor 1205.36.000
FDA UDI
Class IActive
Stem Trial 2015.18.200
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.02.021
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.02.016
FDA UDI
Class IIActive
Klassic HD Acetabular Insert Trial 1204.44.022
FDA UDI
Class IActive
Klassic Femoral Augment, Distal 6402.05.005
FDA UDI
Class IIActive
Klassic All-Poly Tibia, CR/Congruent, Std Poly, size 5 , 16mm 5203.05.016
FDA UDI
Class IIActive
Klassic Stem Extension, Cemented 6600.12.100
FDA UDI
Class IIActive
Tibial Broach Stem 2203.00.075
FDA UDI
Class IActive
Acetabular Insert with ApeX-Lnk Poly, 32mm Head, Size 52mm 3501.52.032
FDA UDI
Class IIActive
Tibial Broach Stem 2203.00.025
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, E-Link 5305.03.010
FDA UDI
Class IIActive
Klassic HD Acetabular Insert with XLPE, 32mm head, size 54mm 3503.54.032
FDA UDI
Class IIActive
Klassic Blade Femoral Stem, Porous, Size 8 3105.08.000
FDA UDI
Class IIActive
Klassic Femoral Augment, Posterior 6401.07.010
FDA UDI
Class IIActive
Platform Neutral Acetabular Insert with E-Link 3511.64.036
FDA UDI
Class IIActive
Klassic BiPolar Head, 54 mm OD, 28 mm Head 3205.54.028
FDA UDI
Class IIActive
Posterior Femoral Augment Trial 2809.03.010
FDA UDI
Class IActive
Tibial Insert Trial, Klassic ONE 2240.03.010
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.03.010
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.04.024
FDA UDI
Class IActive
Hooded Acetabular Insert Trial 1223.56.032
FDA UDI
Class IActive
Distal Femoral Augment Trial 2810.05.010
FDA UDI
Class IActive
Revision Tibial Baseplate Sizer and Trial 2903.04.000
FDA UDI
Class IActive
Tibial Alignment Guide - Lower Tower, Klassic ONE 2233.00.000
FDA UDI
Class IActive
Modular Handle/Alignment Guide, Klassic ONE 2154.00.000
FDA UDI
Class IActive
Tibial Insert Trial 2205.04.016
FDA UDI
Class IActive
Intramedullary Reamer 2014.16.000
FDA UDI
Class IActive
Tibial Baseplate Trial, Pegs, Klassic ONE 2251.05.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.03.010
FDA UDI
Class IIActive
Tibial Insert Trial 2205.01.011
FDA UDI
Class IActive
Klassic BiPolar Trial 1322.48.028
FDA UDI
Class IActive
Stem Trial 2015.20.050
FDA UDI
Class IActive
Klassic HD Modular Femoral Broach 1106.06.000
FDA UDI
Class IActive
Klassic HD Low Profile Acetabular Insert with XLPE Poly 3510.48.032
FDA UDI
Class IIActive
Tibial Stem Extension Reamer 2209.00.100
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.01.016
FDA UDI
Class IIActive
Tibial Broach Stem 2203.00.125
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.05.012
FDA UDI
Class IIActive
Klassic HD Low Profile Acetabular Insert with E-Link Poly 3509.58.032
FDA UDI
Class IIActive
Tibial Stem Extension Reamer 2213.00.000
FDA UDI
Class IActive
Klassic Blade Offset Femoral Stem 3107.11.000
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.01.016
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.01.024
FDA UDI
Class IActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 6 , 14mm 5204.06.014
FDA UDI
Class IIActive
Klassic Tibial Baseplate, Revision 6200.05.000
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (1)

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
Sep 23, 2025Z-0432-2026—open, classified

Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.