# Total Joint Othopedics, Inc.

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 8 (2014–2025): 8 510(k) clearances
- Product codes: JWH (3), LZO (3), LPH (2)
- 510(k) review time since 2016: median 81 days, against 109 for FDA's reviews in the same codes and years (4 of 7 faster)
- Predicates its devices cite: 19 (3 its own); citations of its devices by later devices: 8 (3 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Total Joint Orthopedics, Inc.: 15 (https://510kreport.com/company/total-joint-orthopedics)
- Howmedica Osteonics Corp.: 1 (https://510kreport.com/company/howmedica-osteonics)

## Firms that cite its devices most
- Total Joint Orthopedics, Inc.: 3 (https://510kreport.com/company/total-joint-orthopedics)
- Limacorporate: 1 (https://510kreport.com/company/limacorporate)
- Implantcast GmbH: 1 (https://510kreport.com/company/implantcast)

## Its most-cited devices
- K143407: Klassic HD Hip System (2014), cited by 4
- K230537: Klassic Knee Revision System (2023), cited by 1
- K161073: Klassic HD Hip System (2016), cited by 1
- K213580: Adapter Sleeve for BIOLOX® OPTION Femoral Head, +10.5mm head length (2021), cited by 1
- K243991: Klassic Knee System - Revision Tibial Baseplate (2025), cited by 1

## Recent decisions
- K243991: Klassic Knee System - Revision Tibial Baseplate (Mar 24, 2025)
- K232414: Klassic® Tibial Insert, PS-Post, Klassic All Poly Tibia, PS-Post (Sep 8, 2023)
- K230537: Klassic Knee Revision System (May 19, 2023)
- K213580: Adapter Sleeve for BIOLOX® OPTION Femoral Head, +10.5mm head length (Dec 3, 2021)
- K191399: BIOLOX CONTOURA Ceramic Femoral Head (Aug 28, 2019)
- K171962: Klassic HD® Hip System (Jul 24, 2017)
- K161073: Klassic HD Hip System (Oct 19, 2016)
- K143407: Klassic HD Hip System (Dec 23, 2014)

Source page: https://510kreport.com/company/total-joint-othopedics