Medical Device Manufacturer · US , Anaheim , CA

Hass Corp. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2010

4

Total

4

Cleared

0

Denied

Hass Corp. has 4 FDA 510(k) cleared medical devices. Based in Anaheim, US.

Last cleared in 2021. Active since 2010. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Hass Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Hass Corp.

4 devices

1-4 of 4

Cleared Aug 26, 2021

Amber Mill Q Series & Amber Mill Direct Series

Cleared Jul 14, 2016

Amber Mill Series and Amber Press Series

Cleared Aug 26, 2011

MONOBLOC BM SERIES

Cleared Dec 03, 2010

HASS ZIRTOOTH MODEL ZORTOOTH H. ZIRTOOTH T. ZIRTOOTHC, ZIRTOOTH P