Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of StrykerLabelled by claude-sonnet-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 Gaymar Industries with 27 510(k) clearances. The most recent is a 510(k) clearance dated Jan 20, 2011: MEDI-THERM HYPER/HYPOTHERMIA SYSTEM, MODELS MTA6900, MTA7900.
| Jan 20, 2011 | MEDI-THERM HYPER/HYPOTHERMIA SYSTEM, MODELS MTA6900, MTA7900K100585 · DWJ | 510(k) clearances |
| May 8, 2008 | T-PUMP LOCALIZED TEMPERATURE THERAPY PUMPK073675 · ILO | 510(k) clearances |
| Apr 30, 1997 | CLINIDYNE ROTATIONAL THERAPY MATTRESS SYSTEMK962788 · IKZ | 510(k) clearances |
| Jan 28, 1997 | SOF. PRESS EPC 51 SYSTEMK963067 · JOW | 510(k) clearances |
| Aug 9, 1996 | SPR PLUS II OVERLAY SYSTEM (CL250/CL212K961854 · FNM | 510(k) clearances |
| May 23, 1995 | TC 3000K942881 · DWJ | 510(k) clearances |
| Aug 6, 1993 | TC2000 POWER UNIT AND ACCESSORIESK930345 · DWJ | 510(k) clearances |
| Mar 12, 1992 | SCM-3 AND ACCESSORIESK914921 · IKY | 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
