Amorchem Holdings, Inc. is one of 571 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Amorchem Holdings, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AmorChem Titanium Porous Fixation Device
1
Total
1
Cleared
0
Denied
Amorchem Holdings, Inc. has 1 FDA 510(k) cleared medical devices. Based in Montreal, CA.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Amorchem Holdings, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by BioVera, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Amorchem Holdings, Inc.
1 devices