Medical device makerLabelled 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 Whiteside Biomechanics with 13 510(k) clearances. The most recent is a 510(k) clearance dated Jul 28, 2004: QUATRO M FEMORAL COMPONENT.
| Jul 28, 2004 | QUATRO M FEMORAL COMPONENTK033313 · LWJ | 510(k) clearances |
| May 3, 2002 | SYMMETRIC UNICOMPARTMENTAL KNEE SYSTEMK012800 · HRY | 510(k) clearances |
| May 23, 2001 | WHITESIDE BIOMECHANICS LOW PROFILE STAINLESS STEEL CABLE SYSTEM, MODEL BIO-1-1014K003618 · NDD | 510(k) clearances |
| Feb 14, 2000 | WHITESIDE BIOMECHANICS TITANIUM LOW-PROFILE CABLE, MODEL BIO-1-1013K993903 · JDQ | 510(k) clearances |
| Aug 12, 1999 | WHITESIDE BIOMECHANICS SPINAL SYSTEMK991678 · KWQ | 510(k) clearances |
| Aug 21, 1998 | BIPOLAR FEMORAL HEADK981238 · KWY | 510(k) clearances |
| Nov 24, 1997 | WHITESIDE BIOMECHANICS, INC. CERAMIC UNIPOLAR FEMORAL HEADK973261 · LZO | 510(k) clearances |
| Aug 7, 1997 | QUATROLOC PLASMA SPRAYED FEMORAL COMPONENTK964616 · LPH | 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
