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 Medisiss with 6 510(k) clearances. The most recent is a 510(k) clearance dated Dec 20, 2011: MEDISISS REPROCESSED ARTHROSCOPIC SHAVERS AND BURS.
| Dec 20, 2011 | MEDISISS REPROCESSED ARTHROSCOPIC SHAVERS AND BURSK113028 · HRX | 510(k) clearances |
| Jul 23, 2010 | MEDISSISS REPROCESSEDENT ABLATION WANDS (COBLATORS), MODEL#EIC8872-01K100543 · GEI | 510(k) clearances |
| Aug 28, 2008 | GENESISK081559 · GEI | 510(k) clearances |
| Feb 14, 2005 | MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPSK042659 · NON | 510(k) clearances |
| Jan 23, 2004 | MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTSK030598 · NLQ | 510(k) clearances |
| Jul 3, 2003 | SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND ACCESSORIESK030919 · NLR | 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
