Medical Device Manufacturer · US , Glens Falls , NY

Medi-Dyne, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1993

Recent clearances: 4F-7F MEDI-DYNE TORQ FLOW XLB ANGIOGRAPHIC CATHETER, MEDI-DYNE GUIDING CATHETER, MODIFIED LUER

View 4 510(k) Devices ↓

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Medi-Dyne, Inc. Cardiovascular ✕

4 devices

1-4 of 4

Cleared Sep 21, 2000

4F-7F MEDI-DYNE TORQ FLOW XLB ANGIOGRAPHIC CATHETER

Cardiovascular · 191d

Cleared Aug 01, 1997

MEDI-DYNE GUIDING CATHETER

Cardiovascular · 179d

Cleared Sep 28, 1993

Cardiovascular · 204d

Cleared Aug 02, 1993

MEDI-DYNE ANGIOGRAPHIC CATHETER

Cardiovascular · 173d

Data Source

Sourced from the FDA 510(k) public files . 176,583 total devices indexed.

Last updated: Sep 06, 2026