Medical Device Manufacturer · US , Pittsburgh , PA

Dymax Corp - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1985

Recent clearances: SITE-RITE IV ULTRASOUND SYSTEM, SITE-RITE 3 ULTRASOUND SYSTEM, SITERITE NEEDLE GUIDE (MODIFIED)

View 7 510(k) Devices ↓

7

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Dymax Corp Obstetrics & Gynecology ✕

1 devices

1-1 of 1

Cleared Oct 25, 1989

DYMAX ENDOVAGINAL BIOPSY GUIDE

Obstetrics & Gynecology · 100d

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 11, 2026