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 Smith & NephewLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Dyonics with 19 510(k) clearances. The most recent is a 510(k) clearance dated Feb 16, 1990: MODIFIED USES OF THE ARTHROSCOPIC SURGICAL SYSTEM.
| Feb 16, 1990 | MODIFIED USES OF THE ARTHROSCOPIC SURGICAL SYSTEMK900070 · HRX | 510(k) clearances |
| Jan 2, 1990 | DYONICS SHOULDER PORTAL SYSTEMK896416 · HRX | 510(k) clearances |
| Dec 14, 1989 | SURGI-PAK FOR ARTHROSCOPIC ACROMIOPLASTYK893136 · HRX | 510(k) clearances |
| Nov 3, 1989 | MODIFIED CANNULA, TROCAR AND OBTURATOR ACCESSORIESK890665 · HRX | 510(k) clearances |
| Aug 18, 1989 | DYONICS DISPOSABLE ARTHROSCOPIC SURGICAL KNIFEK894728 · HRX | 510(k) clearances |
| Jun 23, 1989 | PS3500 ARTHROSCOPIC SURGICAL SYSTEMK892062 · HRX | 510(k) clearances |
| Dec 7, 1988 | MODIFIED SAW BLADES TO THE SAGITAL SAWK884839 · KIJ | 510(k) clearances |
| Nov 17, 1988 | DYNAMIC CRUCIATE TESTERK881876 · LYH | 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
