Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list ASI Medical with 5 510(k) clearances and 1 device recall. The most recent is a device recall dated Nov 5, 2013: SEAC Advanced Dental System, Model A591561 The SEAC Advanced Dental System is a self-….
| Nov 5, 2013 | SEAC Advanced Dental System, Model A591561 The SEAC Advanced Dental System is a self-contained dental delivery system with a built-in airClass II · ASI Medical is initiating a field correction for the SEAC Advanced Dental System because the miniature plastic air tank | Device recalls |
| Mar 28, 2013 | ADVANCED ENDODONTIC SYSTEM- DESIGNER SERIESK123139 · ELC | 510(k) clearances |
| Apr 5, 2012 | TRITON SELF CONTAINED DENTAL SYSTEM, TRITON SELF CONTAINED DENTAL SYSTEM, WITH CASEK110481 · EIA | 510(k) clearances |
| May 26, 1998 | AIRPREP SYSTEM - MODEL 9001K974488 · KOJ | 510(k) clearances |
| Feb 18, 1998 | SEAC ADVANCED DENTAL SYSTEM - MODEL 2001,2010 OR MODEL 2020K974487 · EIA | 510(k) clearances |
| Mar 7, 1994 | SEAC MOBILE UNIT BY ASI MEDICALK932873 · EIA | 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
