← 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 12 of 42
DeviceModel / ReferenceRegistriesClassStatus
Screwdriver - Metal Handle 2206.00.100
FDA UDI
Class IActive
Platform Neutral Acetabular Insert with E-Link 3511.50.036
FDA UDI
Class IIActive
Klassic Stem Extension, Cemented 6600.18.200
FDA UDI
Class IIActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 4 , 10mm 5204.04.010
FDA UDI
Class IIActive
Stem Trial 2015.17.040
FDA UDI
Class IActive
Klassic Blade Offset Femoral Stem, Porous, Size 9 3107.09.000
FDA UDI
Class IIActive
Klassic BiPolar Trial 1340.51.028
FDA UDI
Class IActive
Klassic HD Hip System Femoral Stem (12/14 taper), Porous, size 8 3101.08.000
FDA UDI
Class IIActive
Klassic Femoral Augment, Distal 6402.01.010
FDA UDI
Class IIActive
Acetabular Insert with E-Link Poly, 32mm Head, Size 64mm 3502.64.032
FDA UDI
Class IIActive
Klassic Femur with Cobalt 3D, size 7 5102.07.000
FDA UDI
Class IIActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.01.011
FDA UDI
Class IIActive
Klassic Femoral Augment, Posterior 6401.03.010
FDA UDI
Class IIActive
Klassic HD Low Profile Acetabular Insert with E-Link Poly 3509.44.022
FDA UDI
Class IIActive
Stem Trial 2015.14.120
FDA UDI
Class IActive
Klassic HD Neck Trial, Standard 1104.03.000
FDA UDI
Class IActive
Klassic Tibial Insert, Ultra-PS, E-Link Poly 5303.01.014
FDA UDI
Class IIActive
Anteversion Rod for Stem Impactor/Broach Holder 1310.00.000
FDA UDI
Class IActive
Tibial Insert Trial, PS-Post, Klassic ONE 2254.06.021
FDA UDI
Class IActive
Klassic Femoral Augment, Posterior 6401.03.005
FDA UDI
Class IIActive
Tibial Stylus, Threaded 2216.00.000
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Post, E-Link 5305.05.011
FDA UDI
Class IIActive
Klassic HD Modular Femoral Broach 1106.01.000
FDA UDI
Class IActive
Klassic Knee Tibial Insert, CR/Congruent, Size 6, 18 mm, Final Packed, Sterile 5300.06.018
FDA UDI
Class IIActive
Femoral Cut Block, Central Capture, Klassic ONE 2141.05.000
FDA UDI
Class IActive
36mm Femoral Head, 12/14 Taper, +0mm Offset 3200.36.000
FDA UDI
Class IIActive
Klassic Tibial Insert, CR/Congruent, E-Link Poly 5302.05.011
FDA UDI
Class IIActive
Tibial Insert Trial, PS-Post 2224.05.011
FDA UDI
Class IActive
Klassic All-Poly Tibia, Ultra-PS, Std Poly, size 5 , 10mm 5204.05.010
FDA UDI
Class IIActive
32mm BIOLOX delta Femoral Head, 12/14 taper, +3.5mm Head Length 3203.32.350
FDA UDI
Class IIActive
Stem Trial 2015.20.040
FDA UDI
Class IActive
Klassic Blade Femoral Stem, Porous, Size 2 3105.02.000
FDA UDI
Class IIActive
Klassic BiPolar Head, 48 mm OD, 28 mm Head 3205.48.028
FDA UDI
Class IIActive
Klassic BiPolar Trial 1340.58.028
FDA UDI
Class IActive
Klassic Tibial Insert, PS-Max, Std Poly 6300.06.011
FDA UDI
Class IIActive
Acetabular Depth Gage 1215.00.000
FDA UDI
Class IActive
Simple Gap Block, Straight 2222.02.012
FDA UDI
Class IActive
Klassic HD Hooded Acetabular Insert with XLPE Poly 3508.56.032
FDA UDI
Class IIActive
Acetabular Insert with E-Link Poly, 36mm Head, Size 56mm 3502.56.036
FDA UDI
Class IIActive
PS-Post Box Trial 2146.01.000
FDA UDI
Class IActive
Tibial Insert Trial, Klassic ONE 2240.01.014
FDA UDI
Class IActive
Platform Acetabular Cup Sizer 1225.56.000
FDA UDI
Class IActive
Tibial Sizer, Captured Pin, Klassic ONE 2250.05.000
FDA UDI
Class IActive
Universal Cut Block 2102.00.000
FDA UDI
Class IActive
Platform Acetabular Cup with Ti-Coat 3401.56.000
FDA UDI
Class IIActive
Universal Cone Trial, Size 1, 12° 2022.01.012
FDA UDI
Class IActive
Klassic BiPolar X-Ray Template Set 1325.00.000
FDA UDI
Class IActive
Tibial Insert Trial 2205.04.013
FDA UDI
Class IActive
Klassic HD Acetabular Insert with XLPE 3503.44.022
FDA UDI
Class IIActive
PS-Post Box Trial, Klassic ONE 2165.02.000
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.