← 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 25 of 42
DeviceModel / ReferenceRegistriesClassStatus
Klassic Blade Femoral Stem 3105.10.000
FDA UDI
Class IIActive
Modular Broach Holder, Straight 1108.00.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post 2224.04.010
FDA UDI
Class IActive
Klassic BiPolar Trial 1322.58.028
FDA UDI
Class IActive
Platform Acetabular Cup with Ti-Coat 3401.44.000
FDA UDI
Class IIActive
Klassic BiPolar Trial 1340.42.022
FDA UDI
Class IActive
Patella Drill Guide/Sizer, Klassic ONE SRI-10037-01
FDA UDI
Class IActive
Klassic HD Hooded Acetabular Insert with XLPE Poly 3508.46.028
FDA UDI
Class IIActive
Intramedullary Reamer, Revision 2026.10.000
FDA UDI
Class IActive
Klassic Tibial Baseplate with Ti-Coat, size 2 5202.02.000
FDA UDI
Class IIActive
Klassic Tibial Baseplate, Revision 6201.03.000
FDA UDI
Class IIActive
Klassic Knee Tibial Insert, Ultra-PS, Size 3, 16 mm, Final Packed, Sterile 5301.03.016
FDA UDI
Class IIActive
Tibial Sizer and Trial, Klassic ONE 2234.02.000
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.03.016
FDA UDI
Class IIActive
Posterior Femoral Augment Trial 2809.01.005
FDA UDI
Class IActive
Stem Trial 2015.12.120
FDA UDI
Class IActive
Klassic Knee Tibial Insert, Ultra-PS, Size 2, 16 mm, Final Packed, Sterile 5301.02.016
FDA UDI
Class IIActive
Femoral Cut Block, Central Capture, Klassic ONE 2141.02.000
FDA UDI
Class IActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.04.018
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.02.012
FDA UDI
Class IActive
A/P Sizer, Klassic ONE, Pegless 2169.00.000
FDA UDI
Class IActive
Klassic BiPolar Trial 1340.48.028
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, E-Link Poly 5305.05.024
FDA UDI
Class IIActive
Patella Sizer/Drill Guide/Tibial Stem Wrench 2301.00.000
FDA UDI
Class IActive
Klassic HD Hooded Acetabular Insert with E-Link Poly 3507.60.036
FDA UDI
Class IIActive
Hemispherical Acetabular Reamer 1207.42.000
FDA UDI
Class IActive
Tibial Insert Trial, Klassic ONE 2240.03.018
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.03.011
FDA UDI
Class IIActive
Femoral Head Adapter Sleeve for BIOLOX OPTION Femoral Head 3301.00.105
FDA UDI
Class IIActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.01.011
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, E-Link 5305.03.013
FDA UDI
Class IIActive
Platform Hooded Acetabular Insert Trial 1228.62.036
FDA UDI
Class IActive
Stem Trial 2015.19.170
FDA UDI
Class IActive
Klassic Femoral Augment, Posterior 6400.02.005
FDA UDI
Class IIActive
Acetabular Insert Trial 1204.64.036
FDA UDI
Class IActive
Klassic BiPolar Head, 47 mm OD, 28 mm Head 3205.47.028
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, E-Link Poly 5305.06.018
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Post, Std Poly 5304.04.018
FDA UDI
Class IIActive
Klassic HD Acetabular Insert with XLPE, 36mm head, size 62mm 3503.62.036
FDA UDI
Class IIActive
Klassic Knee Tibial Dome Extension 5601.00.000
FDA UDI
Class IIActive
Straight Broach Holder 1101.00.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Max, Klassic ONE 2252.03.018
FDA UDI
Class IActive
Platform Hooded Acetabular Insert with E-Link 3512.64.036
FDA UDI
Class IIActive
Klassic Blade Neck Trial, Standard 1110.04.000
FDA UDI
Class IActive
36mm BIOLOX delta Femoral Head, 12/14 taper, +3.5mm Head Length 3203.36.350
FDA UDI
Class IIActive
Klassic Tibial Baseplate, Revision 6200.03.000
FDA UDI
Class IIActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.03.024
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.05.012
FDA UDI
Class IActive
Hooded Acetabular Insert Trial 1223.58.032
FDA UDI
Class IActive
Tibial Insert Trial, Klassic ONE 2240.02.010
FDA UDI
Class IActive

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.