Medical device makerLabelled 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 13, 2026, FDA's public records list Synectics-Dantec with 19 510(k) clearances. The most recent is a 510(k) clearance dated Jan 29, 1997: PH ANALYSIS MODULE.
| Jan 29, 1997 | PH ANALYSIS MODULEK961346 · FFT | 510(k) clearances |
| Sep 30, 1994 | ZINETICS COMPOSITE SENSOR PROBE W/INTERNAL REF.K925405 · FFT | 510(k) clearances |
| Jun 30, 1994 | MICROTRAPPER/MICRODIGITRAPPER, ADD MODIFICATIONSK924875 · BZQ | 510(k) clearances |
| Dec 13, 1993 | MONOCRYSTANT PH/LES CATHETER, MODIFICATIONK914793 · KLA | 510(k) clearances |
| Jun 18, 1993 | SYNECTICS LIBERTY SYSTEM, PC POLYGRAF/POLYGRAM UROK924383 · FAP | 510(k) clearances |
| Jun 11, 1992 | MONOCRYSTANT PH-REFERENCE CATHETER, MODIFICATIONK913817 · FFT | 510(k) clearances |
| Apr 28, 1992 | PH METER, MODIFICATIONK914624 · FFT | 510(k) clearances |
| Feb 26, 1992 | AIRWAY THERMISTORK914219 · BZG | 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
