FDA Device Intelligence
HomeDevice types › KXA

Prosthesis, Hip, Femoral, Resurfacing

FDA product code KXA · Class 2 · Orthopedic

340
Registered devices
12,332
Adverse events
16
Recalls
23
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2012-09-04Zimmer, Inc.Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Wintetthur, Switz
2010-08-23Depuy Orthopaedics, Inc.As part of our ongoing post-market surveillance of all products, DePuy is continually evaluating data from a variety of sources including national joint replace
2010-08-23Depuy Orthopaedics, Inc.As part of our ongoing post-market surveillance of all products, DePuy is continually evaluating data from a variety of sources including national joint replace
2010-08-23Depuy Orthopaedics, Inc.As part of our ongoing post-market surveillance of all products, DePuy is continually evaluating data from a variety of sources including national joint replace
2010-08-23Depuy Orthopaedics, Inc.As part of our ongoing post-market surveillance of all products, DePuy is continually evaluating data from a variety of sources including national joint replace
2010-08-23Depuy Orthopaedics, Inc.As part of our ongoing post-market surveillance of all products, DePuy is continually evaluating data from a variety of sources including national joint replace
2010-08-23Depuy Orthopaedics, Inc.As part of our ongoing post-market surveillance of all products, DePuy is continually evaluating data from a variety of sources including national joint replace
2010-08-23Depuy Orthopaedics, Inc.As part of our ongoing post-market surveillance of all products, DePuy is continually evaluating data from a variety of sources including national joint replace
2010-08-23Depuy Orthopaedics, Inc.As part of our ongoing post-market surveillance of all products, DePuy is continually evaluating data from a variety of sources including national joint replace
2010-08-23Depuy Orthopaedics, Inc.As part of our ongoing post-market surveillance of all products, DePuy is continually evaluating data from a variety of sources including national joint replace

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.