Orbit Biomedical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Orbit Biomedical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Orbit Subretinal Delivery System
1
Total
0
Cleared
0
Denied
Orbit Biomedical, Inc. has 0 FDA 510(k) cleared medical devices. Based in Ambler, US.
Historical record: 0 cleared submissions from 2018 to 2018. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Orbit Biomedical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Clinreg Consulting Services, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Orbit Biomedical, Inc.
1 devices