Dynarex Corp.
Dynarex Corp. holds FDA 510(k) medical device clearances, first cleared 1986, most recent 2005.
Top product codes for Dynarex Corp.
Recent clearances by Dynarex Corp.
- K052743 — DYNAREX CPR SHIELD WITH ONE WAY VALVE AND BARRIER FILTER, MODEL 4921
- K052314 — DYNAREX VAGINAL SPECULA 4900, MODELS 4911-SMALL, 4912-MEDIUM, 4913-LARGE
- K012816 — DYNAREX IODOFORM PACKING STRIPS, MODELS 3411, 3412, 3413, 3414
- K012957 — TOWEL DRAPE, MODELS 4409, 4410
- K012917 — DYNAREX UMBILICAL CORD LAMP, MODELS 6833 AND 6833-B
- K991694 — DYNAREX DRAIN SPONGE
- K991695 — DYNAREX NON-WOVEN SPONGE
- K983348 — DYNAREX TRACHEOSTOMY SPONGE
- K960388 — DYNAREX NON-WOVEN SPONGE
- K951660 — DYNAREX GAUZE SPONGE
- K933308 — DYNAREX GAUZE SPONGE OR PADS
- K922843 — DYNAREX SUCTION CATHETERS & KITS
- K894686 — POWDER-FREE VINYL EXAMINATION GLOVES
- K893334 — PREPOWDERED VINYL EXAM GLOVES
- K891586 — ORAL AIRWAY
- K882567 — SKINCOTE
- K855130 — TRACHEOSTOMY CARE KIT
- K855132 — SHAVE PREP TRAY
- K855131 — SUTURE REMOVAL KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.