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 Teledyne TechnologiesLabelled 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 Teledyne Getz with 5 510(k) clearances. The most recent is a 510(k) clearance dated Nov 5, 1992: DENSPRO MEDIUM MINT PROPHY PASTE.
| Nov 5, 1992 | DENSPRO MEDIUM MINT PROPHY PASTEK923675 · EJR | 510(k) clearances |
| Nov 5, 1992 | DENSPRO COARSE MINT PROPHY PASTEK923674 · EJR | 510(k) clearances |
| Oct 24, 1990 | SUPER STRENGTH DENTURE ADHESIVE CREAMK903568 · KOT | 510(k) clearances |
| Jun 6, 1990 | SUPER STRENGTH DENTURE ADHESIVE CREAMK901938 · KOB | 510(k) clearances |
| May 15, 1990 | TELEDYNE GETZ'S DISPOSABLE PROPHY ANGLEK901239 · EFB | 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
