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.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Sonotech with 14 510(k) clearances. The most recent is a 510(k) clearance dated Nov 5, 2004: ULTRABIO - IN VIVO BIOCOMPATIBLE, BIOELIMINATED STERILE ULTRASOUND IMAGING COUPLANT.
| Nov 5, 2004 | ULTRABIO - IN VIVO BIOCOMPATIBLE, BIOELIMINATED STERILE ULTRASOUND IMAGING COUPLANTK042619 · MUI | 510(k) clearances |
| Aug 4, 2004 | ULTRABIOK033178 · MUI | 510(k) clearances |
| Jul 23, 2003 | SCANLUBEK031222 · MUI | 510(k) clearances |
| Jul 18, 2003 | SCANTEC PADK031894 · MUI | 510(k) clearances |
| Feb 4, 2002 | ENDO-GLIDEK013701 · GCJ | 510(k) clearances |
| Nov 13, 2001 | SCANTAC MEMBRANE OR SCANTAC STRIPK013170 · ITX | 510(k) clearances |
| Jun 8, 1999 | VIVOSONICK984562 · ITX | 510(k) clearances |
| May 5, 1999 | SCANFLEX SOLID COUPLANT MEMBRANEK983691 · ITX | 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
