Total Joint Orthopedics, Inc.
Total Joint Orthopedics, Inc. holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2026, with 1 FDA device recall on record.
Top product codes for Total Joint Orthopedics, Inc.
FDA recalls by Total Joint Orthopedics, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Total Joint Orthopedics, Inc.
- K261734 — Klassic Infection Spacer System
- K220483 — Platform® Acetabular System
- K211877 — Klassic Knee System
- K211602 — Klassic Knee System
- K202740 — Klassic Knee System Tibial Inserts, PS-Max
- K183596 — Klassic Knee System - Klassic Knee PS-Post Femur +2 more
- K190280 — Klassic Knee System - Sombrero Patella with Standard Poly, Klassic Knee System - Sombrero Patella with E-Link Poly
- K180929 — Klassic HD® Hip System
- K180159 — Klassic® Knee System
- K173104 — Klassic HD® Hooded Acetabular Insert with E-Link® Poly, Klassic HD® Low Profile Acetabular Insert with E-Link® Poly
- K162422 — Klassic Knee System
- K162256 — Klassic Femur, Porous, Klassic Tibial Baseplate, Porous
- K153310 — Klassic Knee System
- K153075 — Klassic Knee System
- K151440 — Klassic HD Hip System
- K150105 — Klassic Knee System-Sombrero Patella
- K141972 — KLASSIC HD ACETABULAR INSERT WITH E-LINK POLY
- K140942 — KLASSIC KNEE TIBIAL STEM EXTENSION
- K133832 — KLASSIC HD HIP SYSTEM, OFFSET FEMORAL STEM, NON-POROUS / POROUS
- K131454 — KLASSIC HD(TM) EXTENDED OFFSET FEMORAL HEAD
- K112906 — KLASSIC KNEE SYSTEM
- K100445 — KLASSIC HD HIP SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.