Optmed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Optmed, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BondEase 2 Topical Skin Adhesive, TearRepair Liquid Skin Protectant
3
Total
3
Cleared
0
Denied
Optmed, Inc. has 3 FDA 510(k) cleared medical devices. Based in New York, US.
Latest FDA clearance: Sep 2025. Active since 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Optmed, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by RQM+ as regulatory consultant.
FDA 510(k) Regulatory Record - Optmed, Inc.
3 devices