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.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Richard's Medical Equipment with 48 510(k) clearances. The most recent is a 510(k) clearance dated Jun 16, 1983: PATIENT GUIDED ELBOW & SHOULDER EXERC.
| Jun 16, 1983 | PATIENT GUIDED ELBOW & SHOULDER EXERCK830793 · BXB | 510(k) clearances |
| Mar 29, 1983 | RMC TOTAL KNEE SYSTEMK823837 · MBV | 510(k) clearances |
| Mar 9, 1983 | SPECTRON NECK REPLACEMENT PROSTHESISK823724 · JDI | 510(k) clearances |
| Mar 9, 1983 | SPECTRON CONVERSION ENDOPROSTHESIS CUPK823726 · KWY | 510(k) clearances |
| Mar 9, 1983 | SPECTRON PROXIMAL FEMORAL PROSTHESISK823723 · JDI | 510(k) clearances |
| Mar 8, 1983 | SPECTRON LONG, STRAIGHT FEMORAL PROSTHESK823722 · JDI | 510(k) clearances |
| Mar 8, 1983 | SPECTRON PRIMARY STEM FEMORAL PROSTHESK823727 · JDI | 510(k) clearances |
| Feb 28, 1983 | RICHARDS INTRA-ARTICULAR SHAVER BLADESK830153 · GEY | 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
