Hass Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hass Corp. - FDA 510(k) Cleared Devices
Recent clearances: Amber Mill Q Series & Amber Mill Direct Series
5
Total
5
Cleared
0
Denied
Hass Corp. has 5 FDA 510(k) cleared medical devices. Based in Anaheim, US.
Latest FDA clearance: Jun 2026. 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.
510(k) submissions have been managed by LK Consulting Group USA, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Hass Corp.
5 devices
Cleared
Jun 11, 2026
Rosetta SM, Rosetta SP
Dental
87d
Cleared
Aug 26, 2021
Amber Mill Q Series & Amber Mill Direct Series
Dental
330d
Cleared
Jul 14, 2016
Amber Mill Series and Amber Press Series
Dental
177d
Cleared
Aug 26, 2011
MONOBLOC BM SERIES
Dental
81d
Cleared
Dec 03, 2010
HASS ZIRTOOTH MODEL ZORTOOTH H. ZIRTOOTH T. ZIRTOOTHC, ZIRTOOTH P
Dental
109d