Is this your brand? Sign in to claim ownership.

TOTAL JOINT ORTHOPEDICS, INC.

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 11 of 42

Device	Model / Reference	Registries	Class	Status
Distal Femoral Cut Guide	2101.00.000	FDA UDI	Class I	Active
Acetabular Shell with Ti-Coat, 56mm	3400.56.000	FDA UDI	Class II	Active
Tibial Insert Trial, PS-Post	2224.05.014	FDA UDI	Class I	Active
Hemispherical Acetabular Reamer	1207.62.000	FDA UDI	Class I	Active
Fixed Distal Femoral Cut Guide, Klassic ONE	2156.00.006	FDA UDI	Class I	Active
Cancellous Bone Screw with 6.5mm Head Diameter, 45mm	3600.45.065	FDA UDI	Class II	Active
Stem Trial	2015.19.120	FDA UDI	Class I	Active
Klassic Femoral Augment, Posterior	6401.04.010	FDA UDI	Class II	Active
Intramedullary Reamer	2014.12.000	FDA UDI	Class I	Active
Tibial Insert Trial, Klassic ONE	2240.02.011	FDA UDI	Class I	Active
Universal Cone System Instrumentation Tray	2416.00.000	FDA UDI	Class I	Active
Intramedullary Reamer	2014.18.000	FDA UDI	Class I	Active
Tibial Insert Trial	2205.06.016	FDA UDI	Class I	Active
Hooded Acetabular Insert Trial	1223.46.022	FDA UDI	Class I	Active
Hooded Acetabular Insert Trial	1223.46.032	FDA UDI	Class I	Active
Intramedullary Reamer	2014.17.000	FDA UDI	Class I	Active
Tibial Insert Trial, PS-Post	2224.03.010	FDA UDI	Class I	Active
Stem Trial	2015.13.170	FDA UDI	Class I	Active
Tibial Insert Trial	2205.06.012	FDA UDI	Class I	Active
Klassic Femur with Aurum	5104.05.000	FDA UDI	Class II	Active
Patella Trial	2303.01.000	FDA UDI	Class I	Active
Klassic Knee Tibial Baseplate Assembly, Size 2	5200.02.000	FDA UDI	Class II	Active
Tibial Insert Trial, PS-Post, Klassic ONE	2254.06.012	FDA UDI	Class I	Active
Stem Trial	2015.10.150	FDA UDI	Class I	Active
Hemispherical Acetabular Reamer	1207.60.000	FDA UDI	Class I	Active
Klassic HD Hooded Acetabular Insert with E-Link Poly	3507.44.022	FDA UDI	Class II	Active
Simple Gap Block, Straight	2222.05.010	FDA UDI	Class I	Active
Klassic HD Hip Offset Femoral Stem Trial	1316.04.000	FDA UDI	Class I	Active
Klassic Knee Tibial Stem Extension, 125mm	5600.00.125	FDA UDI	Class II	Active
Hooded Acetabular Insert Trial	1223.52.032	FDA UDI	Class I	Active
Stem Trial	2015.10.120	FDA UDI	Class I	Active
Platform Neutral Acetabular Insert with E-Link	3511.50.032	FDA UDI	Class II	Active
Klassic Tibial Insert, Ultra-PS, E-Link Poly	5303.02.018	FDA UDI	Class II	Active
Klassic Stem Extension, Cemented	6600.16.200	FDA UDI	Class II	Active
Tibial Insert Trial	2205.05.013	FDA UDI	Class I	Active
Tibial Alignment Guide - Lower Tower	2200.00.000	FDA UDI	Class I	Active
Klassic Knee Domed Patella, Size 2	5500.02.000	FDA UDI	Class II	Active
Platform Hooded Acetabular Insert with E-Link	3512.56.036	FDA UDI	Class II	Active
Femoral Trial, PS-Post/Revision	2126.04.000	FDA UDI	Class I	Active
Tibial Sizer	2202.04.000	FDA UDI	Class I	Active
Tibial Insert Trial, PS-Post, Klassic ONE	2254.05.018	FDA UDI	Class I	Active
Klassic Tibial Insert, PS-Max, Std Poly	6300.06.010	FDA UDI	Class II	Active
Tibial Insert Trial, PS-Post, Klassic ONE	2254.02.013	FDA UDI	Class I	Active
Modular Femoral Head Trial	1326.36.035	FDA UDI	Class I	Active
Klassic Knee Femur, Revision	6100.03.000	FDA UDI	Class II	Active
Hemispherical Acetabular Reamer	1207.61.000	FDA UDI	Class I	Active
Klassic Tibial Insert, PS-Post, E-Link	5305.04.010	FDA UDI	Class II	Active
Stem Trial	2015.11.100	FDA UDI	Class I	Active
Femoral Cut Block, Narrow	2139.07.000	FDA UDI	Class I	Active
Femoral Trial, PS-Post/Revision	2126.07.000	FDA UDI	Class I	Active

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.

Date	Recall No.	Class	Status	Reason
Sep 23, 2025	Z-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.