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 Matrix Medica, Inc. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Sep 18, 1996: FLEXSCOPE.
| Sep 18, 1996 | FLEXSCOPEK961536 · GDB | 510(k) clearances |
| Jan 23, 1996 | KLORMANK923693 · LRJ | 510(k) clearances |
| Oct 28, 1994 | MATRX HOPE(R) 5 RESUSCITATORK921982 · BTM | 510(k) clearances |
| Dec 27, 1991 | MATRX MEDICAL MAXIMIZER 1000 AND 2000 VACUUM PUMPK915353 · EIA | 510(k) clearances |
| Aug 21, 1991 | MATRX, PYRAMID TRIANGLE BANDAGEK912661 · ILI | 510(k) clearances |
| May 9, 1990 | MATRX DISPOSABLE NON-INVASIVE GELLED PACING ELEC.K900551 · DRS | 510(k) clearances |
| Jan 26, 1990 | MATRX BATTERY CHARGER/DEFIBRILLATOR TESTERK895525 · DRL | 510(k) clearances |
| Jan 26, 1990 | LIFE DEFENSE PLUS(TM), DEFIBRILLATOR/MONITOR/PACERK895533 · LDD | 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
