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 Arbor Technologies, Inc. with 10 510(k) clearances. The most recent is a 510(k) clearance dated Apr 4, 1997: SYRINGEFILTER.
| Apr 4, 1997 | SYRINGEFILTERK960928 · BSN | 510(k) clearances |
| Jan 22, 1997 | AUTOPRIMEK964283 · FPB | 510(k) clearances |
| Mar 22, 1994 | PRESSURE TUBING AND ACCESSORIESK922777 · HIF | 510(k) clearances |
| Apr 23, 1991 | ANESTHESIA CONDUCTION FILTERK902666 · BSN | 510(k) clearances |
| Feb 7, 1991 | CONTAIN(TM)K895859 · GCX | 510(k) clearances |
| Jan 4, 1991 | CONTAIN(TM) LASER PLUME FILTERK902167 · JDY | 510(k) clearances |
| Jun 7, 1989 | MICROSEPT 60/20K890844 · CAK | 510(k) clearances |
| May 20, 1988 | CONTAIN(TM)K874505 · GCX | 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
