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 Zimmer BiometLabelled 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 Electro-Biology with 28 510(k) clearances. The most recent is a 510(k) clearance dated Oct 8, 1999: EBI OMEGA 21 SYSTEM.
| Oct 8, 1999 | EBI OMEGA 21 SYSTEMK992333 · MNI | 510(k) clearances |
| Sep 23, 1999 | EBI XFIX DYNAFIX SYSTEM HA COATED SCREWSK992367 · HWC | 510(k) clearances |
| Aug 19, 1999 | EBI XFIX DFS RAIL SYSTEMK991941 · KTT | 510(k) clearances |
| Apr 29, 1999 | EBI SPINELINK ANTERIOR CERVICAL SPINAL SYSTEMK991092 · KWQ | 510(k) clearances |
| Apr 29, 1999 | EBI OMEGA 21 SYSTEMK990303 · KWP | 510(k) clearances |
| Apr 23, 1999 | EBI VUECATH ENDOSCOPIC SYSTENK990459 · HRX | 510(k) clearances |
| Apr 14, 1999 | MODIFICATION OF: EBI SPINELINK SYSTEMK990999 · MAI | 510(k) clearances |
| Jan 19, 1999 | EBI SPINELINK SYSTEMK984027 · MNI | 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
