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 14, 2026, FDA's public records list Andronic Devices with 16 510(k) clearances. The most recent is a 510(k) clearance dated Nov 21, 1994: INSIGHT ELECTRONIC ALIGNMENT INDICATOR.
| Nov 21, 1994 | INSIGHT ELECTRONIC ALIGNMENT INDICATORK940812 · KQX | 510(k) clearances |
| May 26, 1994 | INSITE MODEL 20 & MODEL 15 INSUFFLATORSK934926 · HIF | 510(k) clearances |
| May 26, 1994 | INSITE FILTER & TUBING SETK934928 · HIF | 510(k) clearances |
| Apr 15, 1994 | KAPS POSITIONING ARMK935381 · FWZ | 510(k) clearances |
| Apr 13, 1994 | AUTOQUOT AUTOMATED ALIQUOTTING SYSTEMK934124 · JQW | 510(k) clearances |
| Mar 31, 1994 | ENDEX ENDOSCOPIC POSITIONING SYSTEMK936308 · FQO | 510(k) clearances |
| Feb 3, 1994 | ARTHROBOT BI-FOLD DRAPEK932253 · KKX | 510(k) clearances |
| Oct 19, 1992 | ADEPT ENDOSCOPIC POSITIONERK922625 · GAD | 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
