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 Dentsply SironaLabelled by claude-sonnet-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 Cavitron Corp. with 32 510(k) clearances. The most recent is a 510(k) clearance dated Jul 28, 1981: THE PLACER.
| Jul 28, 1981 | THE PLACERK811582 · EID | 510(k) clearances |
| Feb 13, 1981 | MINOR SURGERY LIGHTK810207 · GBC | 510(k) clearances |
| Dec 17, 1980 | SPIROMETRIC COMPUTER #SC-10K802928 · BZC | 510(k) clearances |
| Nov 18, 1980 | CAVITRON ULTRASONIC SURG. ASPIR. CUSAK801623 · LFL | 510(k) clearances |
| Sep 16, 1980 | SLIT LAMP ATTACHMENTK801877 · HQB | 510(k) clearances |
| May 28, 1980 | MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALAK800869 · CCK | 510(k) clearances |
| Apr 29, 1980 | AUTO-FIELD D AUTOMATED VISUAL DETECTORK800722 · HPT | 510(k) clearances |
| Sep 19, 1979 | MODEL G-61 ULTRASONIC DENTAL UNITK791585 · ELC | 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
