Heany Industries, Inc. is one of 18459 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Heany Industries, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Luxisse+, HEANY INDUSTRIES INC DENTAL XIRCONIA
2
Total
2
Cleared
0
Denied
Heany Industries, Inc. has 2 FDA 510(k) cleared medical devices. Based in Scottsville, US.
Historical record: 2 cleared submissions from 2008 to 2015. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Heany Industries, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Group as regulatory consultant.
FDA 510(k) Regulatory Record - Heany Industries, Inc.
2 devices