Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of DJO GlobalLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list DJO Surgical with 1 510(k) clearance and 1 device recall. The most recent is a device recall dated Feb 7, 2014: FMP X-alt Acetabular Liner This acetabular liner is intended for use with DJO Surgica….
| Feb 7, 2014 | FMP X-alt Acetabular Liner This acetabular liner is intended for use with DJO Surgical hip systems. It is used with an acetabular shell tClass II · Packaging error -- two different types and sizes of acetabular liners used during hip replacement surgery were mistakenl | Device recalls |
| Oct 27, 2009 | REVERSE SHOULDER PROSTHESISK092873 · PHX | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
