Medical Device Manufacturer · US , Albuquerque , NM

Avanca Medical Devices, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2005

Recent clearances: PROCEDUR-10, PROCEDUR 10 SYRINGE DEVICE, PROCEDUR SF SAFETY SYRINGE DEVICE

View 3 510(k) Devices ↓

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Avanca Medical Devices, Inc. General Hospital ✕

3 devices

1-3 of 3

Cleared Nov 09, 2005

General Hospital · 100d

Cleared Jan 21, 2005

PROCEDUR 10 SYRINGE DEVICE

General Hospital · 130d

Cleared Jan 21, 2005

PROCEDUR SF SAFETY SYRINGE DEVICE

General Hospital · 130d

Data Source

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

Last updated: Sep 25, 2026