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 Johnson & JohnsonLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record. See the Johnson & Johnson group view.
As of Nov 14, 2026, FDA's public records list DePuy with 316 510(k) clearances and 11 device recalls. The most recent is a device recall dated May 19, 2026: Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Insert Components with the below product….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| May 19, 2026 | Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Insert Components with the below product descriptions and Part Codes. 1. ATTUNE KNEE SYSTClass II · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. | Device recalls |
| May 19, 2026 | Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Housing Components with the below product descriptions and Part Codes. 1. ATTUNE KNEE SYSClass II · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. | Device recalls |
| Apr 3, 2026 | Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 8 CEM. Part Number: 150450108.Class II · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. | Device recalls |
| Apr 3, 2026 | Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 5 CEM. Part Number: 150450105.Class II · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. | Device recalls |
| Apr 3, 2026 | Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 5 CEM. Part Number: 150450205.Class II · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. | Device recalls |
| Apr 3, 2026 | Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 8 CEM. Part Number: 150450208.Class II · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. | Device recalls |
| Apr 3, 2026 | Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 7 CEM. Part Number: 150450107.Class II · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. | Device recalls |
| Apr 3, 2026 | Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 3 CEM. Part Number: 150450203.Class II · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. | Device recalls |
| Jan 19, 2022 | GLOBAL ICON Stemless Shoulder SystemK212683 · PKC | 510(k) clearances |
| Feb 24, 2020 | DELTA XTEND(TM) Reverse Shoulder SystemK192855 · PHX | 510(k) clearances |
| Nov 1, 2019 | DePuy Corail AMT Hip ProsthesisK190344 · LZO | 510(k) clearances |
| Oct 8, 2019 | Attune Revision LPS InsertsK191779 · KRO | 510(k) clearances |
| Oct 4, 2019 | Delta Xtend Revers Shoulder SystemK192448 · PHX | 510(k) clearances |
| May 17, 2019 | Delta Xtend Reverse Shoulder SystemK183077 · PHX | 510(k) clearances |
| Jun 15, 2017 | ATTUNE Cemented Tibial Base, Fixed BearingK170806 · JWH | 510(k) clearances |
| Jul 19, 2016 | DePuy Actis DuoFix Hip ProsthesisK160907 · MEH | 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
