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 Thermo Fisher ScientificLabelled 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 14, 2026, FDA's public records list Sybron Corp. with 37 510(k) clearances. The most recent is a 510(k) clearance dated Jun 23, 1986: SEALITE.
| Jun 23, 1986 | SEALITEK862284 · EBC | 510(k) clearances |
| Jan 30, 1986 | PROOF ALGINATE IMPRESSION MATERIALK854855 · ELW | 510(k) clearances |
| Oct 25, 1984 | DIAGNOSTIC MICROSOPCE SLIDESK844092 · | 510(k) clearances |
| Jul 18, 1984 | TYCOS SELF-CHECK/DIGITAL FEVER THERMOK842132 · FLL | 510(k) clearances |
| Jul 13, 1984 | KERR SEALAPEX ROOT CANAL SEALERK841910 · EJK | 510(k) clearances |
| Jun 5, 1984 | LIEBEL-FLARSHEIM AFC 1000 X-RAY FILMK841732 · IZP | 510(k) clearances |
| May 21, 1984 | TYCOS SELF CHECK BPM3 BLOOD PRESS MONIK840469 · DXN | 510(k) clearances |
| May 21, 1984 | KERR RESIN BONDED BRIDGE CEMENTK840407 · EMA | 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
