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 2 spellings of its name, each linked to the record. See the Johnson & Johnson group view.
As of Nov 15, 2026, FDA's public records list DePuy Synthes with 20 510(k) clearances. The most recent is a 510(k) clearance dated Aug 1, 2024: DePuy Synthes Retrograde Femoral Nail Advanced System.
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.
| Aug 1, 2024 | DePuy Synthes Retrograde Femoral Nail Advanced SystemK233696 · HSB | 510(k) clearances |
| Jun 17, 2024 | CROSSNAV Navigation Enabled InstrumentsK233255 · OLO | 510(k) clearances |
| Jun 17, 2024 | Robotic Integration InstrumentsK233256 · OLO | 510(k) clearances |
| Jun 14, 2024 | TELIGEN System Navigation Ready InstrumentsK233254 · OLO | 510(k) clearances |
| Mar 21, 2024 | DePuy Synthes VOLT Mini Fragment Plating System, DePuy Synthes VOLT Small Fragment Plating SystemK233665 · HRS | 510(k) clearances |
| Jul 26, 2023 | DEPUY SYNTHES MAXFRAME AUTOSTRUT SystemK231922 · KTT | 510(k) clearances |
| Sep 20, 2022 | DePuy Synthes 3.5mm Intrapelvic Acetabular SystemK221809 · HRS | 510(k) clearances |
| Mar 18, 2022 | DePuy Synthes Radial Head Replacement SystemK213563 · KWI | 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
