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 15, 2026, FDA's public records list Apex Medical Technologies with 8 510(k) clearances. The most recent is a 510(k) clearance dated May 24, 2012: RHEA CUP.
| May 24, 2012 | RHEA CUPK112165 · HHE | 510(k) clearances |
| May 9, 2006 | SOLACE POST-OPERATIVE PAIN RELIEF INFUSION SYSTEMK060933 · MEB | 510(k) clearances |
| Jan 5, 1996 | SEMINAL FLUID COLLECTION KIT IIK954791 · HIS | 510(k) clearances |
| May 4, 1995 | EXTRA PROTECTION POLYURETHANE CONDOMK922688 · MOL | 510(k) clearances |
| Mar 18, 1993 | APEX SPECIMEN BAGK930313 · LIO | 510(k) clearances |
| Mar 6, 1991 | POLYURETHANE CONDOMK902936 · HIS | 510(k) clearances |
| Mar 1, 1989 | SENSATIONS BRAND CONDOMSK871358 · HIS | 510(k) clearances |
| Dec 14, 1987 | HI-TOUCH (TM) BRAND SURGICAL GLOVESK874539 · KGO | 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
